Submit the form on the right to access your copy of the July 2017 SeerPharma Journal and read the following stories:
3 Pharmaceutical Processing Problems that Data Alone Couldn't Solve
Assisting Medical Device company with navigating new Medical Device Regulation (MDR) in Europe
SeerPharma QA Contract Resources for Pharmaceutical and Medical Device companies
Working closely with Traditional Chinese Medicine (TCM) manufacturers in Singapore
At Singapore Polytechnic
SeerPharma assisting early stage researchers with masterclass on regulatory pathways
SeerPharma in discussion with clients on providing assistance with IT Projects in a Regulated Environment
What's new in the PE 009-13 PIC/S Guide to GMP
Navigating the pathway of TGA enforcement of the PIC/S Guide to GMP for Medicines
SeerPharma is a team of consultants that provide advice, training, IT solutions and contract labour resources to pharmaceutical, medical device, life science manufacturers and other regulated industries in the Asia-Pacific region on Quality Assurance and GMP compliance.
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