SeerPharma have been invited by the Stevanato Group and Lonza to present on Pharmaceutical Quality Management System Certification at The Innovative Solutions for Pharmaceutical Packaging Roadshow in Singapore.
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Recent Posts
Application of ISO 14971 Risk Management to New Medical Devices
The stages required for applying ISO 14971 principles to risk management for medical devices can be typically broken into 6 steps:
Experience from Attending Master of GMP Course at UTS
UTS International student Tong Zhao is a Pharmacy graduate from Liaoning Province, China, currently undertaking the Master of Good Manufacturing Practice here in the UTS Graduate School of Health. We sat down with Tong to hear her story.
Computer System Validation: Starting on the Right Track
Most of us follow a professional sporting team. Each year we start the season with hope and enthusiasm that ‘this year’ will be ‘our year’. Have our recruiters and management assembled the right mix of youth and experience and will they be coached to their strengths? Is the framework in place to raise our odds of success ?
Developing an Advanced Manufacturing Process
Australian biotech company VivaZome Therapeutics has announced that it has been awarded an Australian Government CRC-P grant of $2.18m in support of the project “Enabling Exosome Therapy: Developing an Advanced Manufacturing Process”, with the funds provided under the Advanced Manufacturing Scheme.
Infographic: QA & GMP Compliance Performance Snapshot for 2017
INFOGRAPHIC: A snapshot of how SeerPharma has supported its clients in 2017 on matters of QA and GMP compliance.
SeerPharma Sponsoring and Exhibiting at BioLogistics World Asia 2018
The launch of new temperature sensitive biologics, increasing regulations, growing cost- pressures are putting more complex demands on the biopharma industry’s high-stakes logistics environment.
SeerPharma Sponsoring & Exhibiting @ Biologics Manufacturing Asia 2018
The biologics manufacturing industry has undergone several changes over the past few years starting from the development of better expression systems to modular and flexible manufacturing facilities including the emergence and use of disposables. However, there is a need for higher productivity with upstream process development and cost-effective...
TGA Update: Transition to PIC/S GMP Guide PE 009-13
The TGA has published details of the 12 month graduated transition period to PIC/S Guide to GMP PE 009-13, commencing 01 January 2018. The key changes and a transition plan have been summarised in tables by chapter and appendix and are linked here for your convenience.
Online GMP Training Helps 10,000 People
SeerPharma reached a milestone this quarter with the 10,000th trainee going through our cloud-based online GMP training, "E-learning".