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SeerPharma Blog

SeerPharma to Deliver Bioprocessing Training Programs at UTS

February 19, 2020

The University of Technology Sydney (UTS) recently opened its Biologics Innovation Facility (BIF). The 430 square meter facility houses a series of clean rooms and containment laboratories meeting cGMP codes. The facility has been set up to provide the biotech and pharmaceutical sector with an opportunity to have their employees locally trained...

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Infographic: QA & GMP Compliance Performance Snapshot for 2019

January 08, 2020

INFOGRAPHIC:  A snapshot of how SeerPharma supported its clients in 2019 on matters of Quality Assurance and GMP compliance.

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PIC/S Guide to GMP Training for PT Kalbio Global Medika in Indonesia

April 27, 2018

Kalbe Farma is a leading healthcare provider in Indonesia, with extensive operations throughout the South East Asian region. Its’ subsidiary PT Kalbio Global Medika (KGM) has recently opened a new 11,000 square meter factory in Indonesia, which received a Honourable Mention for the 2017 Facility of the Year Awards from ISPE.

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Infographic: QA & GMP Compliance Performance Snapshot for 2017

January 03, 2018

INFOGRAPHIC:  A snapshot of how SeerPharma has supported its clients in 2017 on matters of QA and GMP compliance.

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Infographic: QA & GMP Compliance Performance Snapshot for 2016

March 02, 2017

INFOGRAPHIC:  A snapshot of how SeerPharma has supported its clients in 2016 on matters of QA and GMP compliance.

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Cell Therapies Training with CRC for Cell Therapy Manufacturing

December 21, 2016

Cell therapies are an emerging form of healthcare that have started to produce transformative outcomes for patients with previously refractory diseases, but they are substantially more complex than small molecule or biologic drugs and present significant challenges for researchers and companies in cell therapy translation.

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GMP Coaching Program Assists Biopharmaceutical Manufacturer

November 11, 2016

A biopharmaceutical manufacturer engaged SeerPharma to provide on-going coaching to their Quality personnel and advise on improvements to help prepare for a FDA inspection.

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GMP Data Integrity Masterclass

September 14, 2016

GMP Data Integrity is an issue that a number of our clients have approached us about recently. The concept of Data Integrity has been around for quite some time, with the TGA introducing the concept of electronic records in to the previous Australian code of GMP back in 1990, while the FDA made 21 CFR Part 11 Electronic records and signatures...

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Pharmaceutical Manufacturers Association Recommends G(QC)LP Services

September 05, 2016

One of our senior consultants in Singapore, received the following glowing recommendation from the Sri Lanka Pharmaceutical Manufacturers' Association (SLPMA) which is a testament to the quality of our team in Singapore who continually strive to deliver exceptional service to customers in the region.

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Good Distribution Practice (GDP) Training in Asia

June 28, 2016

 Zuellig Pharma is Asia’s leading healthcare service provider offering a broad range of innovative services including distribution of pharmaceuticals, medical devices, special solutions and other healthcare related consumer products.

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