Regulatory -

November 29, 2022
Medicinal Products,
Pharmacovigilance
Importance of Qualified Person for Pharmacovigilance (QPPV) and Local Responsible Person (LRP)
November 24, 2022
Medical Devices,
EU Compliance
Key Considerations for Successful Creation and Submission of a 510(k) eCopy
November 21, 2022
Medicinal Products,
Regulatory Affairs
Understanding China’s Patent Linkage System and Its Impact on Drug Registration
October 21, 2022
Medical Devices,
Digital Health
Top FAQs about Medical Device Single Audit Program (MDSAP)
August 30, 2022
Medical Devices,
Regulatory Affairs
An Exclusive Webinar - Foundation Masterclass: 510(k) Clearance Pathway
May 20, 2022
Medicinal Products,
Publishing and Submission
Promotional Material – FDA’s Electronic and Non-electronic Format Submission Guidance
November 26, 2019
Medicinal Products,
Labeling
TGA Assessed Claim on Medicine Labels - What You Need to Know?
January 28, 2019
Medical Devices,
Regulatory Affairs
TGA’s Draft Guidance for Medical Device Cyber Security - Regulatory Insights for Industry & Highlights
December 24, 2018
Medicinal Products,
Regulatory Affairs
Artificial Intelligence (AI) in Life Sciences Roadblocks and Current Applications
November 15, 2018
Food Supplements
Nutraceuticals in the Global Arena & The Strategies Manufacturers Should Work On
November 9, 2018
Cosmetics
ANVISA’s Simplified Regulations for Children Cosmetics. Decode.
August 30, 2018
Cosmetics
4 Key Aspects to Register/Notify Cosmetics in Brazil