ICPGGRA2020
10th International Conference on Pharmaceutical GMP, GCP & Regulatory Affairs 2020
Important Dates
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
Topics
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 regulationsCall 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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