10th International Conference on Pharmaceutical GMP, GCP & Regulatory Affairs 2020

Vancouver, Canada, Canada
19 - 20 October 2020
8 days since the conference ended

Important Dates

Abstract Submission Deadline
23rd September 2020
Abstract Acceptance Notification
23rd September 2020
Final Abstract / Full Paper Deadline
28th September 2020

About ICPGGRA2020

We feel delighted to host the "10th International Conference on Pharmaceutical GMP, GCP & Regulatory Affairs" during October 19-20, 2020 at Vancouver, Canada


Self-regulation, Regulations of nanotechnology, Drugsafety, Pharmacovigilance and its significance, Regulatory affairs, Drugs acting on copd, Clinical pharmacology and bio pharmaceutics, Pharma., Drug development, Drug targeting and design, Regulatory requirements for pharmaceuticals, Smart drug delivery systems, Regulatory issues and biosafety challenges in bioanalysis., Biological and pharmaceutical sciences, Food safety laws and regulations, Clinical practice, Legislation and regulatory capacities, Biopharmaceuticals, Intellectual property rights, Biopharmaceutics & biotherapeutics, Biopharmaceuticals & nutraceuticals, Global regulatory intelligence, Marketing authorizations, Pharma marking, Regulatory non-compliance, Softwares in gmp and gcp, Medical devices and combination product regulations

Call for Papers

We feel delighted to welcome everyone to attend our forthcoming 10th International Conference on Pharmaceutical GMP, GCP & Regulatory Affairs which is going to place during October 19-20, 2020 in the beautiful and exciting city of Vancouver, Canada. The theme runs on Regulatory Challenges and implications in Pharmaceutical Biopharmaceutical Research and Market.

Regulatory Affairs 2020 focuses on the importance of Pharmaceutical Industry. It is the revenue generator for pharmaceutical Industry. It is an established event attracting global participant’s intent on sharing and exploring new avenues in Pharmaceutical Biopharmaceutical research & Market, related research, and the latest developments. It includes plenary speakers, established Keynote speakers, active Invited speakers, fresh contributed speakers, and Young Researchers. In addition, a variety of poster presentations along with workshops, symposiums, and special sessions would be interested in the audience.

Conference Highlights:

Regulatory Affairs

Clinical and Regulatory Affairs

Biologics and Biosimilars

Global Regulatory Intelligence

Regulatory Affairs in Pharmacovigilance

Regulatory Strategies and developments

Penalties for Regulatory Non-compliance

Marketing Authorizations

Regulatory Challenges for Medical Devices

Medical Devices and Combination Product Regulations

Best Industry Practices

Intellectual Property Rights

GMP in Food Industry

Impact of Brexit on Regulatory Framework

Current GMP Guidelines cGMP GxP in Pharmaceuticals

Role in cGMP

Good Clinical Practices

Good Laboratory Practices

Softwares in GMP and GCP

Regulatory Communications and Submissions

Regulatory Requirements for Pharmaceuticals

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