Please visit the updated page of Clinical Trial Conferences to attend by year


As the Clinical Trial space grows throughout North America, so does industry events. Everything from vendor selection to clinical trial operational effectiveness to regulatory concerns are available. This industry has a tremendous amount of events throughout the year.

Instead of recommending the typical top 20 list, our sister site ComplyDocs published the most comprehensive list of 87 conferences and events taking place in North America for 2019 specific to the Clinical Trial, Clinical Research, Pharma and Regulatory sectors. In chronological order, here’s our list:



87 Clinical Trial, Pharma & Regulatory Conferences to attend in North America for 2019





January 22 – January 23 14th Biosimilars Summit Alexandria, VA
Join CBI’s 14th Biosimilars Summit and explore the current global climate for biosimilars, evaluate competition and benchmark with industry peers on how to navigate the changing regulations and landscape of the biosimilars market.
January 22-24th, 2019 8th Trial Master File Summit  Orlando, FL
The 8th Annual Trial Master File Summit is taking place on January 22-24 at the Hilton Orlando Lake in Buena Vista, Orlando Florida. The conferences cover a range of topics related to TMFs, eClinical Systems and Trial Master File Processes with presentations from some of the industry’s most notable specialists and experts. If you are involved in clinical documentation management or Trial Master Files, this is an essential North American conference to attend.
January 28-29th, 2019 2nd Innovative Regulatory Pathways Summit Arlington, VA
ExL’s 2nd Innovative Regulatory Pathways will serve as a platform to discuss and compare the current regulatory pathways that allow for earlier attention to drugs that have promise in treating serious or life-threatening conditions.
January 29-30th, 2019 18th Annual Bio/Pharma Contact Centers Philadelphia, PA
CBI’s 18th Annual Bio/Pharma Contact Centers conference is the bio/pharmaceutical industry’s must-attend event for those responsible for medical communications, medical information, customer relations and contact center management
January 29-30th, 2019 4th Annual Medical Affairs Excellence Forum Philadelphia, PA
CBI’s 4th Annual Medical Affairs Excellence Forum to learn more about the evolving role of medical affairs. New demands for scientific information, coupled with compliance pressures and requests for data, contribute to an exciting era.
Feb 5 – 6, 2019 6th Annual Rare Disease Market Access & Commercialization Summit Philadelphia, PA
6th Annual Rare Disease Market Access & Commercialization Summit is organized by World Congress and will be held from Feb 05 – 06, 2019 at Hilton Philadelphia at Penn’s Landing, Philadelphia, Pennsylvania, United States of America.
February 6-7th, 2019 IISR 2019 — 7th Annual Investigator Initiated Sponsored Research Summit Boston, MA
CBI’s Investigator Initiated Sponsored Research Summit is the only annual event dedicated exclusively to helping you and your organization improve your IISR programs by providing innovative and forward-thinking approaches to support collaborative partnerships, address budgeting and contracting challenges, improve data management and quality assurance and integrate best practices in clinical operations
February 6 -7th, 2019 10th Annual Pharma Market Research Conference Newark, NJ
The prestigious 10th Annual Pharma Market Research Conference (Feb 6-7, 2019, New Jersey) is the best and largest industry assembly of market research executives in pharma, biotech, medical devices & diagnostics. Meet 300+ pharma/biotech industry influencers and decision makers. Hear from 75+ senior-level speakers in 50+ sessions. Advance your career. Enjoy 10th Anniversary prizes, games and celebrations
February 11 – 13th, 2019 Regulatory Submissions, Information, and Document Management Forum North Bethesda, MD
DIA’s Regulatory Submissions, Information, and Document Management Forum  is the key place to engage with expert speakers and your peers to better understand these topics, as well as discover ways in which the integration of data, documents, and knowledge can be leveraged to develop insights and enable better business decisions.
February 12th – 13th, 2019 Outsourcing in Clinical Trials West Coast 2019 Burlingame, CA
Arena International’s flagship Outsourcing in Clinical Trials West Coast conference returns to the Bay Area for its 11th year in February 2019.

With 6 tracks spanning across 2 days, the 2019 event is guaranteed to provide you with practical takeaways to help you accelerate your clinical trial timelines as well as insider knowledge on new innovations and technological advancements in the industry.

February 19th -20th, 2019 CHI’s 9th Annual Protocol Development, Global Site Selection, Feasibility and Site Management Orlando, FL
Data-driven global site selection, an optimized protocol development and feasibility assessment process, and effective site management are critical to improving clinical trial timelines and outcomes. Too often companies fail to learn from past mistakes and take the same approach to trial planning and execution. In order to overcome challenges in clinical trial planning, operations and site management leaders should learn from the best practices of their peers, utilize data and analytics to support decision making, and improve communication and relationships between Sites, CROs, and Sponsors. CHI’s 9th Annual “Protocol Development, Global Site Selection, Feasibility and Site Management” will cover the topics one should consider when planning and implementing a trial.
February 27-28th, 2019 7th Annual Compliance Monitoring Forum 2019 Philadelphia, PA
CBI’s 7th Annual Compliance Monitoring Congress, leading industry experts convene to discuss the challenges of expanding compliance monitoring efforts to address growing areas of risk with limited resources.
February 28th-1st March, 2019 Advertising and Promotion Regulatory Affairs Conference North Bethesda, MD
The conference, which has taken place annually for 30 years, delivers a multi-stakeholder perspective on new FDA guidances and the latest enforcement, the challenges of marketing pharmaceuticals and medical devices in a mobile-first world, and new technologies relevant to the promotion of FDA-regulated products. Industry and government thought leaders will facilitate interactive, forward-looking discussions that will shape policy, advance understanding, and define strategic priorities within the ad promo regulatory space.
March 3rd–6th, 2019 13th Clinical Trial Billing & Research Compliance Conference Orlando, FL
The 13th Clinical Trial Billing and Research Compliance conference is a stand alone conference for the billing compliance and reimbursement teams at both physician practices, hospitals, university medical centers, and both pharmaceutical and device industry partners! Learn how to take some of the best practices of your peers and improve your billing compliance process. You will learn what to expect from claims processing, denials and proper budgeting.
March 4th- 8th, 2019 Biotherapeutics Analytical Summit Alexandria, VA
The industry-recognized Biotherapeutics Analytical Summit has come to be known as THE analytical event developed by, and for analytical scientists. Each year, we bring together regulatory and standards agencies, industry and academia to showcase current trends, new guidelines, robust technologies, innovative concepts, practical approaches and best practices that can help companies advance their molecules from discovery to development and commercialization.
March 7-8th, 2019 CRO Partnerships & Oversight Excellence Boston, MA
CBI’s CRO Partnerships & Oversight Excellence brings pharma startups, large pharma and CROs together to optimize clinical partnerships. This program gives you a chance to learn everything you need to ensure first-time partnerships are well-matched, optimized and clear of bottlenecks. Benchmark with peers to gain strategies to evaluate and implement best practices that will ensure your trials stay on time and on budget.
March 11th-13th, 2019 Integrated Pharma Informatics San Francisco, CA
The pharmaceutical industry plays a key role in driving informatics for translational research and precision medicine. The 11th Annual Integrated Pharma Informatics program will discuss the challenges related to integrating, analyzing, and interpreting data from clinical trials, sequencing, electronic health records, and wearables. We will discuss informatics strategy for entire organizations from business goals to infrastructure and storage projects. Special attention will be paid to artificial intelligence, machine learning, natural language processing, and how companies are integrating these tools into their informatics infrastructure.
March 12-14th, 2019 4th Annual Medical Device Validation Week Minneapolis, MN
IVT’s 4th Annual Medical Device Validation Week is the must-attend event for quality, validation and design control professionals in medical device and diagnostics companies to benchmark with industry leaders and peers to improve current validation practices.
March 18-20th, 2019 10th Proactive GCP Compliance Summit Philadelphia, PA
Now in its tenth year, ExL’s Proactive GCP Compliance conference continues to act as the annual forum for senior-level clinical quality and clinical operations executives to gather, learn and discuss strategies to achieve and maintain global GCP compliance. Join ExL to learn how to effectively build quality risk management approaches into your clinical operations to optimize research, maintain GCP compliance, contain costs and ensure patient safety.
March 18 – 20th, 2019 Medical Affairs and Scientific Communications Forum Orlando, FL
DIA’s Medical Affairs and Scientific Communications Forum is designed for medical affairs professionals, by medical affairs professionals. This forum provides a comprehensive understanding of the regulatory and compliance environment directly affecting the daily activities of medical affairs and scientific communication professionals. Made up of multiple general sessions and four breakouts sessions within three tracks covering medical communications, medical writing, and medical science liaisons, you can pick and choose which sessions to attend and create your own unique meeting.
March 18 – 19th, 2019 2nd Adaptive Clinical Trials Symposium Philadelphia, PA
Adaptive clinical trial design allows for modifications to the trial after it begins without damaging the integrity of the study. An adaptive design allows for a more proficient use of capital and resources through shorter timeframes and fewer patients. Using adaptive design sponsor organizations can allocate resources more efficiently without lowering standards and therefore are able to accelerate the clinical development process.
March 20- 21th, 2019 FDA Clinical Trial Requirements, Regulations, Compliance and GCP Conference Newport Beach, CA
This two-day conference is intended to share information among FDA representatives and the regulated community, to facilitate the understanding of regulations, guidelines and practices, and to suggest methods and opportunities to enhance the research professional’s product development experience. The program will focus on the relationships among the FDA and clinical trial staff, investigators and IRBs. The workshop will highlight three areas that present challenges to sponsors and investigational sites: FDA Clinical Research Requirements, Enhancing Success through Communication and Financial Incentives, and Assuring Confidence in Clinical Research.
March 24-27th, 2019 Pharma Forum 2019 New York City, NY
15 years of experience in meeting management training, Pharma Forum pushes the limits on the caliber of cutting-edge, educational programming. Featuring engaging and informative keynote speakers, brimming with industry experts in educational breakout sessions, showcasing the latest technologies and incorporating the most impactful networking experiences, Pharma Forum 2019 is destined to exceed your highest expectations.
March 25 – 26th, 2019 The 2nd Pharmacovigilance Audit and Inspections Conference Philadelphia, PA
ExL’s 2nd Pharmacovigilance Audit and Inspection Conference will focus on the best practices and strategies for those preparing for their audit and inspection, educating PV professionals on new technologies and innovative methods in pharmacovigilance that are emerging, and how to utilize them to improve organizational performance and reporting.
March 26th & 27th, 2019 Clinical Trial Supply New England 2019 Boston, MA
We will once again be meeting in to discuss, deliberate and debate the latest operational and technological challenges with regards to clinical trial supplies. Over the course of two days you can expect to catch-up with old colleagues and make new lasting business connections to help drive success in your trials. As Arena’s dedicated Clinical Trial Supply conference for the New England area, this event caters to local needs while offering the change to meet international sponsors and solution providers.
March 26th & 27th, 2019 Outsourcing in Clinical Trials Southeast 2019 Durham, NC
This year’s Outsourcing in Clinical Trials Southeast event builds on last year’s incredibly successful conference, which will be returning to North Carolina with the aim of supporting trial sponsors and solution providers in the RTP and neighboring regions.
March 27 -28th 2019 Clinical Trials Ontario Conference Toronto, ON
Clinical trials are continuing to evolve as new technology and approaches to research come onto the scene. Speakers at this year’s conference will discuss how we can improve clinical trials today while preparing the ground for an even stronger clinical trials environment in the future.
April 1st – 2nd, 2019 3rd Clinical Trial Financial Management Summit Philadelphia, PA
Managing clinical trial finances is an ongoing challenge throughout the entirety of a study. Each trial is unique in its inception, and therefore budgets can be difficult to forecast and control. Operational decisions made by stakeholders can affect the finances of a trial in a multitude of ways, often causing a study to go over budget and over time. The success of any study is contingent on the effective collaboration of a sponsor, research site and a CRO.
April 2 – 4th, 2019 Interphex 2019 New York, NY
For 40 years, INTERPHEX has proven to be the place to find all of the State-of-the-Art Solutions you need to Cost Effectively Develop and Manufacture Quality Product. INTERPHEX is the premier pharmaceutical, biotechnology, and device development and manufacturing event where you can “Experience Science through Commercialization”. Based in New York, INTERPHEX brings over 11,000 global industry professionals and 650+ leading suppliers together to “Learn It, Experience It, Procure It” through a combination of no cost technical conference, exhibits, demonstrations, and networking events to leverage quality, efficiency and cost effectiveness in today’s ever-changing global market.
April 4-5th, 2019 13th Annual Device Research & Regulatory Conference Newport Beach, CA
This two day conference will focus on device regulatory basics and address prior year attendee topic requests, new technology, medical advances, as well as new or updates to regulations, standards and guidance. Attendees will hear from and discuss issues with experts from FDA, site, industry, and clinical research support organizations in the medical device research and regulatory fields.
April 8th-10th, 2019 DIA/FDA Biostatistics Industry and Regulator Forum North Bethesda, MD
The DIA/FDA Biostatistics Industry and Regulator Forum is focused on statistical thinking to inform policy, regulation, development, and review of medical products in the context of the current scientific and regulatory environments including pharmaceuticals, biologics and biosimilars, combination products and devices, and generics. Each session will be co-chaired by an FDA/Industry team working side-by-side with today’s experts to present a 360-degree perspective of statistical design, analysis, and methodological approaches to building evidence for pharmaceutical, biologic and biosimilar, combination product and device development, and approval.
April 12–April 15th, 2019 Association of Clinical Research Professionals Meeting & Expo Nashville, TN
ACRP 2019 brings the clinical research community together to learn, connect, and explore opportunities to drive excellence in clinical research.

The premier education and networking event for clinical research professionals, ACRP 2019 is the ideal venue for learning the practical strategies, best practices, and creative solutions needed to improve clinical trial quality.

April 16-18th, 2019 BioIT World Boston, MA
Since its debut in 2002, the Annual Bio-IT World Conference & Expo has established itself as a premier event showcasing the myriad of IT and informatics applications and enabling technologies that drive biomedical research, drug discovery & development, and clinical and healthcare initiatives. The Bio-IT World Conference & Expo continues to be a vibrant event that unites 3,000+ life sciences, pharmaceutical, clinical, healthcare, and IT professionals from more than 30 countries.
April 16-18th, 2019 16th Annual Pharmaceutical Compliance Congress Washington, DC
The largest and most power-packed event for compliance professionals in the bio/pharmaceutical industry returns for the most in depth and impactful event yet! Backed by 15 years of high quality content, PCC 2019 is the industry’s gold standard for compliance excellence, attracting more than 500 industry leaders annually.
April 28th- May 1st, 2019 16th Annual World Health Care Congress Wshington, DC
WHCC19 brings together global thought leaders and key decision-makers from all sectors of the health care ecosystem to connect, learn, and share best practices in an elite networking forum resulting in an exchange of valuable strategies
April 30th-May 1st, 2019 11th Annual Clinical Trial Budgeting and Forecasting Philadelphia, PA
CBI’s 11th Annual Clinical Trial Budgeting & Forecasting conference to identify solutions and best practices for ensuring accurate and effective budgeting, forecasting and management of clinical trials.
April 30th & May 1st 2019 Clinical Operations in Oncology Trials West Coast 2019 Burlingame, CA
6th Annual Clinical Operations in Oncology Trials to the West Coast on April 30th-May 1st 2019. As one of the only oncology operationally focused events in the West Coast, this meeting will aim to provide strategies to allow for operationally meaningful and targeted oncology trials to engage West Coast physicians and patients.
April 30th-May 3rd, 2019 FDA/Xavier MedCon Conference 2019 Cincinnati, OH
FDA/Xavier MedCon brings the global medical device community together to openly discuss the most pressing issues facing our industry. You have the opportunity to influence decisions and have your voice heard as you interact with leading FDA officials and field investigators, along with global industry experts.
May 5 – May 8 MAGI Clinical Research Conferences Boston, MA
MAGI holds two Clinical Research Conferences per year: one in the Spring in the eastern U.S. and one in the Fall in the western U.S. 100+ sessions and workshops in six tracks: clinical operations & project management, site management, regulatory compliance, contracts, budgets & billing, and special topics. Over 800 people (including representatives from over 100 sponsors and CROs) will attend.
May 7th, 2019 Outsourced Pharma Conference & Exhibition Boston, MA
Outsourced Pharma Conference & Exhibition is a vibrant forum for thought-leadership and the application of best practices for professionals engaged in outsourcing drug development and manufacturing. These conferences and exhibitions form a community for networking and discussing topics most relevant to sponsor-provider partnerships and supply-chain management, within an open format that promotes panel and attendee interaction.
May 13-15th, 2019 CHI’s Clinical Trial Innovation Summit Boston, MA
Cambridge Healthtech Institute’s Clinical Trial Innovation Summit brings together leaders from across pharma, biotech and academia to share case studies and best practices on effective clinical trial management and vendor oversight. The program focuses on key issues and opportunities in the clinical trial industry, including Patient Recruitment, Site Selection, Data Integration, Existing Data Sources, Mobile Tech, Project Management, Outsourcing, Vendor Management, Budgeting and Contracting, Quality (QbD) in Trial Conduct, Risk-Based Monitoring and Clinical Auditing.
May 14 – 15th, 2019 TMF Summit San Francisco, CA
The work of TMF professionals is evolving in complexity at the same time as it is growing in significance. Individuals and companies must adapt to keep pace with the changing regulations, emerging technologies, the advent of the eTMF, the growth of CROs in marketplace, globalization among a plethora of other stressors. Companies are leveraging eTMFs and other evolving technologies for the quality management systems and for monitoring trials for Inspection Readiness
May 15-16th, 2019 U.S. Based Global Transparency Reporting Congress Philadelphia, PA
CBI’s 2nd Annual U.S.-Based Global Transparency Reporting Congress offers compliance professionals an interactive forum to examine the latest trends, challenges and solutions for navigating the dynamic global transparency reporting environment.
May 19-22nd, 2019 Society for Clinical Trials 40th Annual Meeting New Orleans, LA
The Annual Meeting of the Society for Clinical Trials is a multidisciplinary program with broad participation. The Meeting brings together the clinical trials community from academia, the pharmaceutical and device industries, government agencies, medical groups, centers and clinical research entities.
May 20–21th, 2019 6th Due Diligence Summit for Life Sciences Philadelphia, PA
The 6th Due Diligence Summit for Life Sciences, taking place on May 20–21, 2019, in Philadelphia, PA, is the industry’s leading cross-functional life science event focused on the needs of due diligence professionals. This conference will highlight the latest M&A trends in the market, educate due diligence professionals on the different aspects and challenges faced by cross-functional team members, and provide attendees with the strategies and insight they need to effectively conduct thorough due diligence to ensure a profitable investment in a new product, portfolio, company or strategic alliance.
May 21th-22th, 2019 Neurotech Investing & Partnering Conference Boston, MA
Its 14th year, the Neurotech Investing & Partnering Conference (being held May 21-22, 2019 at the Renaissance Waterfront Hotel in Boston, MA) is the premier business and investment conference for commercial neuroscience including pharmaceuticals, medical devices, diagnostics and neurosoftware. The conference features keynotes, investor panels, cutting edge company presentations, and panel discussions on a comprehensive selection of neurotech topics. Our goal is to provide a highly-interactive environment where cutting edge technologies, devices, drugs and therapies inspire new collaborations and secure financing to navigate the development path and ultimately reach patients.
May 21 – 22th, 2019 Clinical Trial Risk Management Seminar San Francisco, CA
Clinical Trial Risk Management Seminar provides a comprehensive education on clinical risk management and the tools to assess, maintain and mitigate risk to ensure compliance. Join us on May 21–22 in San Francisco for this exciting gathering of clinical quality, compliance and operations executives from the leading biopharma companies, service providers and sites.
May 23-24th, 2019 Neuro National Clinical Trial Training Program Montreal, Quebec
The Montreal Neurological Institute and Hospital’s Clinical Research Unit (CRU), will hold its 4th Annual Neuro National Clinical Trial Training Program on May 23 & 24, 2019 at the Montreal Neurological Institute and Hospital.  Principal investigators, researchers, clinical research coordinators, and representatives from industry are invited to attend this two-day program covering education and training on: clinical trial readiness, medical monitoring, CROs, novel technology in clinical trials, consortium trials, trial design, drug safety, clinical trial outcome measures, and more.
May, 2019 2nd Maximizing Investigator Meetings Philadelphia, PA
Investigator meetings are essential to successfully train clinical sites as they directly affect a sponsor’s ability to collect accurate safety and efficacy data. A well-executed investigator meeting cultivates a crucial team atmosphere and is an opportunity for sites and sponsors to discuss the protocol, regulatory issues, enrollment criteria, and procedures. Having the opportunity to discuss protocol specific subjects directly with the sponsor is of great value for clinical sites.
June 03rd-06th, 2019 BIO International Convention Philadelphia, PA
The BIO International Convention, organized by the Biotechnology Industry Organization will take place from 3rd June to 6th June 2019 in Philadelphia, United States Of America. The conference will cover areas like business development & finance, biomedical technology: research & development, digital health, general biotechnology interest, intellectual property and value, market access & commercialization.
June 6-7th, 2019 Conducting Clinical Trials in Canada Conference Toronto, ON
Conducting Clinical Trials in Canada will be accomplished through lecture and practical application facilitated by clinical research professionals. Information will be presented and discussed regarding the administration of clinical trials according to Health Canada Regulations and International Conference on Harmonisation (ICH) guidelines as well as practical procedures and site / sponsor / CRO relationships.
June 11-13th, 2019 Pharmaceutical Compliance Congress Canada Toronto, ON
CBI’s 3rd Annual Pharmaceutical Compliance Congress Canada convenes top Canadian compliance practitioners and leading experts to discuss effective strategies to achieve organization-wide compliance, from the compliance and legal teams to the oversight of the promotional marketing and sales teams. Join your Canadian colleagues for robust conversations on the top issues facing industry today.
June 12-13th, 2019 Rare Disease Innovation and Partnering Summit Boston, MA
CBI’s Rare Disease Innovation Summit brings together diverse stakeholders to discuss the most pressing challenges to successful market access and commercialization. The summit provides a unique opportunity to share best practices and lessons learned in this complex but exciting environment. Benefit from hearing about the experiences of industry, advocates and patients on successful collaboration on accelerated approvals and increased patient access.
June 12-13th, 2019 15th Annual Medical Device Compliance Congress Chicago, IL
CBI’s 15th Annual Medical Device Compliance Congress (MDCC) serves as the industry’s premier compliance event for medical device and diagnostics professionals. This must-attend conference unites senior-level compliance professionals to discuss the latest enforcement trends and compliance challenges, including global regulatory compliance requirements, enforcement and investigation developments, privacy and cybersecurity challenges, anti-corruption best practices and much more.
June 17-20th, 2019 World Pharma Week 2019 Boston, MA
World Pharma Week will bring together a unique and international mix of large and medium pharmaceutical and biotech companies, CROs, leading universities and clinical research institutions, emerging companies and tool providers—making it a perfect meeting-place to share experience, foster collaborations across industry and academia, and evaluate emerging technologies.
June 23 – 27th, 2019 DIA 2019 Global Annual Meeting San diego, CA
The DIA 2019 Global Annual Meeting brings together thousands of innovators from around the globe. Designed to drive insights into action by connecting key policy discussions to real-world knowledge that you need to do your job every day, your attendance will accelerate your growth and your organization’s performance in the development ecosystem.
June 24 – 26th, 2019 9th Digital Pharma West San Francisco, CA
At Digital Pharma West, we will explore these themes, delve into relevant questions and provide solutions to help overcome obstacles in your everyday business.
June, 2019 (exact date TBC) 8th Annual Regulatory Operations & Submission Publishing Strategies Conference Arlington, VA
This conference will build on knowledge share and successes of past years. The 2019 program will showcase industry experts in regulatory operations and publishing, who will share experiences and knowledge that will be of great benefit to all attending delegates. All content is delivered by life science industry speakers as case studies, panels, and traditional presentations so attendees will leave with tangible ideas that may be implemented immediately.
July 8-9th, 2019 eRegulatory Submissions Summit Philadelphia, PA
eRegulatory Submissions Summit examines updates in documentation submissions to regulatory agencies in order to clarify the applications and identify best practices for electronic submissions. It will cover changes made to the electronic submission processes and protocols for constructing strategies for IDMP, RIM, global and regulatory submissions. This summit will also address regulatory information management experiences and the standards for the identification of medicinal products and best practices for eCTD submission requirements.
July 8–9th, 2019 3rd eRegulatory Submissions Summit Philadelphia, PA
The 3rd eRegulatory Submissions Summit will cover changes made to the electronic submission processes and protocols for constructing strategies for IDMP, RIM, global and regulatory submissions. This summit will also address regulatory information management experiences and the standards for the identification of medicinal products and best practices for eCTD submission requirements.
July 9-July 11, 2019 11th Annual AACI CRI Meeting Chicago, IL
The AACI Clinical Research Inititative (CRI) Annual Meeting is designed to support leaders of cancer center clinical trials offices as they work to improve the clinical research process, understand the global impact of conducting clinical research in the United States and abroad, discuss trends in clinical trial safety and compliance, and recommend policies to promote staff retention at the cancer centers.
July 10th– 11th, 2019 Outsourcing in Clinical Trials : Medical Devices USA 2019 Irvine, CA
Arena International is delighted to announce OCT Medical Devices USA will be returning to Orange county in 2019 for another superb year. We have explored the latest regulatory challenges for medical device manufacturers and building relationships between sponsors and vendors to facilitate the formation of new partnerships and strengthening existing relationships.
July 19-20, 2019 8th International Conference on Clinical Trials Atlanta, USA
8th International Conference on Clinical Trials to be held in Atlanta, USA during July 19-20, 2019. The Conference brings together Academicians, Researchers, Doctors, Principle Investigators, Clinical research sites, CROs, CMOs, Investors, and senior executives from Biotech, Biopharma, Biomedical, Medical devices and Pharmaceutical industries around the globe to discuss, reflect on and develop their ideas. It offers many opportunities for professional contact and development, and is a great networking event.
July 29th – 31st, 2019 Clinical Trial Billing Compliance Boot Camp Chicago, IL
Clinical Trial Billing Boot Camp in the country with training by an experienced clinical team who has build coverage analysis for over ten years! The strategy of the Boot Camp is for your clinical trial billing team to learn the basics, understand the billing compliance process, and gain knowledge from networking. Learn how to build a coverage analysis and with the tools to validate the national Guidelines, National Coverage Decisions and Local Coverage Decisions.
August 2-3rd, 2019 9th International Conference on Pharmaceutical GMP, GCP, & Regulatory Affairs Chicago, IL
2019 Key Themes Regulatory Affairs 2019 conference will focus on new strategies, amendments, innovations, developments in the fields of regulatory affairs, intellectual property rights and medical devices with the theme: “Current challenges of Pharmaceutical & Biopharmaceutical Industries in regulatory framework” which reflects new strategies in the field of regulatory affairs.
August 12 – 13th, 2019 3rd Disclosure and Transparency for Clinical Data Summit Philadelphia, PA
ExL’s 3rd Disclosure and Transparency for Clinical Data Summit attendees will gain comprehensive, high-quality education that balances commercial values and ethical responsibility through the execution of national and global data transparency.
August 14-15th, 2019 Direct-to-Patient Clinical Trials Philadelphia, PA
CBI’s Direct to Patient Clinical Trials returns to help you work through your biggest hurdles protocol, operationalization, data management, device validation, procurement and cost management among many other topics.
September 9-12th, 2019 Biotech Week Boston 2019 Boston, MA
Biotech Week Boston 2019 is a conference and exhibition dedicated to discoveries, clinical development, financing, and manufacturing in the biotechnology and life sciences industries. Biotech Week Boston 2019 brings together scientists, executives, investors, technologists and more.
September 11-12th, 2019 5th Annual Compliance Congress for Specialty Products Boston, MA
CBI’s 5th Annual Compliance Congress for Specialty Products is the life science industry’s only conference catered to the unique compliance challenges for specialty pharmaceutical companies pre- and post-commercialization.
September 17-18th, 2019 DPharm: Disruptive Innovations Conference  Boston, MA
DPharm is a TED-style annual event to get the best access to innovative and disruptive ideas to advance drug development operations from pharma and outside industry leaders with a view to reducing the burden to patients and investigators. Now in its 8th year, DPharm is dedicated to all things digital, data science, patient data ownership and new approaches to optimize clinical operation systems. The 2018 event saw over 400+ participants from mid to large pharma, biotech companies, patient groups, investors, as well as CROs and Sites.
September 19th-20th, 2019 Clinical Trial Disclosure and Data Transparency Conference Bethesda, MD
Clinical trial information transparency is taking on new dimensions. Clinical trial sponsors and academia are facing a host of new registration requirements in the US and the EU. With evolving requirements comes a host of new challenges, creating additional opportunities for knowledge-sharing and necessitating more interaction with peers. This conference will provide critical and timely information relating to clinical trial disclosure and data transparency from those on the front lines.
September 21-24th, 2019 RAPS Regulatory Convergence Philadelphia, PA
RAPS is a gathering of the global regulatory community for the healthcare products industry. It brings together professionals from all domains of the life sciences in order to share the latest industry knowledge, network and learn more about the new things that are happening at the FDA, EMA, Health Canada and more ministries of health around the world.
September 23-24th, 2019 Rare Diseases and Orphan Drugs Conference Toronto, Ontario
Rare Diseases 2019 provides a premier interdisciplinary platform for researchers to present the latest research findings and describe emerging technologies, and directions in rare diseases and orphan drugs issues. The conference seeks to contribute to presenting novel research results in all aspects of Rare Diseases and Orphan Drugs. The conference will focus on evidence-based benefits proven in clinical trials and scientific experiments.
September 27- Sep 29, 2019 SOCRA Annual Conference San Antonio, TX
For the 28th year, SOCRA will welcome clinical research professionals from across the world. Located in San Antonio, TX at the Grand Hyatt San Antonio, this three day conference will offer current information and tools, best practices, and training to assure that you’re up-to-date and compliant in your clinical research practice. The program will feature over 100 academic sessions, a peer-driven poster session, and an exhibit program.
September 29-October 2nd, 2019 Society for Clinical Data Management Annual Conference Baltimore, MD
The Society for Clinical Data Management (SCDM) international organization of 2,400+ members worldwide was founded to advance the discipline of clinical data management on multiple fronts: technological, regulatory, procedural and personnel. The upcoming event is one of the largest educational events for clinical data managers and related professionals coming from more than 27 different countries including CDM leadership, pharma and biotech companies, CROs, and vendors.
October 2nd – 3rd, 2019 Clinical Trial Supply Southeast 2019 Durham, NC
The Clinical Trial Supply Southeast event offers attendees a unique opportunity to debate and develop practical strategies that will enable their company, whether big or small, to improve the efficiency of its clinical trial supply chain. We encourage interaction throughout the event and seek to develop an open arena for information sharing and networking.
October 11th – 13th, 2019 2019 Global Site Solutions Summit Hollywood, FL
For the last 13 years, the Global Site Solutions Summit has been committed to being “the site’s meeting.” The Summit provides a unique hub where sites, sponsors, CRO executives and regulators come together and share best practices, build their businesses, and develop new partnerships through debates, ideation sessions, workshops and focus groups.

SCRS is confident that by increasing site sustainability, all life science stakeholders will realize greater efficiency and profitability, and successfully meet our ultimate commitment to bring safe medical treatments to patients faster.

October 15-16th, 2019 CRO Advancement Summit TBA
CRO Advancement Summit will bring together operations professionals from Pharma and CRO firms to collaborate on issues that are commonly faced during the execution and management of clinical trials. Experts will facilitate conversations regarding contract models and negotiation, communication and transparency standards, timeline management and risk mitigation to enhance stakeholders’ ability to streamline operations and drive efficiency.
October 16-17th, 2019 Basket & Umbrella Trials for Clinical Oncology Philadelphia, PA
CBI’s Basket and Umbrella trials returns as the leading event to help you ensure clinical success by adopting new trial formats, learning to operationalize trials, mastering legal hurdles, gaining strategies for patient recruitment, and designing cutting edge trial protocols.
October 22nd and 23rd, 2019 Outsourcing in Clinical Trials Pacific Northwest 2019 Seattle, WA
Outsourcing in Clinical Trials Pacific Northwest Event were given the chance to hear from expert speakers from key companies in the Northwest region including Seattle Genetics, Pharmacyclics, Aquinox Pharmaceuticals and Impel NeuroPharma, as well as networking opportunities with a host of innovative solution-providers.
October 29th – 30th, 2019 Clinical Trial Supply Midwest 2019 Chicago, IL
The Clinical Trial Supply Midwest conference will return for its 4th year to Chicago, Illinois on 29th – 30th October 2019; the only co-located event with Outsourcing in Clinical Trials conference in Midwest area. this conference addressed how life science companies can effectively streamline clinical supply process to ensure timely and cost-effective clinical studies and be responsive to industry trends to enable early market penetration.
November 4th, 2019 Canadian Pharmacovigilance and Risk Management Conference Gatineau, QC
DIA’s Canadian Pharmacovigilance and Risk Management Strategies Conference is the premier place to hear from expert pharmaceutical, biotechnology, and regulatory personnel. The latest updates in pharmacovigilance, risk management, and drug safety will be presented from both a global and a tailored Canadian perspective.
November 4-5th, 2019 Investigator-Initiated Studies Forum Philadelphia, PA
Investigator-initiated research is highly important for successfully answering important medical and scientific questions, which will uncover solutions to unmet therapeutic needs. These solutions can lead to a successful study that can improve patient care and spark new ideas for further disease-related research that will produce improved medicines for people who need them.
November 5th-6th, 2019 DIA Annual Canadian Meeting Gatineau, QC
The DIA Annual Canadian Meeting will deliver a comprehensive overview of the current bio-pharma and device landscape in Canada, while sharing insights into Canada’s broader role in global healthcare product development. From policy updates and priorities shared directly from Health Canada, to sessions on international work sharing and partnerships to key regulatory and clinical considerations for drugs and devices, you will have the exclusive opportunity to address the current issues and opportunities in Canada and across the globe.
November 6th – 8th , 2019 20th Annual Pharmaceutical & Medical Device Compliance Congress Washington, DC
The Pharmaceutical Compliance Forum (PCF) is a not-for-profit membership organization for Compliance and Legal professionals from pharmaceutical and biotechnology manufacturers. The mission of the organization is to promote effective compliance programs through education, networking, and sharing of current best practices. The Congress is the oldest and largest gathering of pharma and device compliance professionals and in-house counsel who come together annually to discuss best practices in legal and regulatory compliance.
November 13th – 14th, 2019 RBM Risk-Based Trial Management & Monitoring Philadelphia, PA
CBI’s Risk-Based Trial Management and Monitoring conference is dedicated to reducing the complexity of implementing an efficient RBM methodology and refining processes while providing real-world strategies to system adoption and process integration.
December 10-11th, 2019 Clinical Trial Legal and Contracting Forum Philadelphia, PA
CBI’s Clinical Trial Agreement Series announces CBI’s Clinical Trial Legal and Contracting Forum that serves as the only meeting that is singularly focused on the detailed legal and contracting issues that relate to clinical agreements of all types.
December 10-12th, 2019 The FDA/CMS Summit Washington, D.C.
FDA/CMS Summit will cover areas like Updates on the latest drug review statistics from the Office of New Drugs and industry’s experience under the new review Program and outlook for biopharma under the new health care exchanges.