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SeerPharma Welcomes 2020 Cohort of Postgraduate GMP Students at UTS

March 02, 2020

SeerPharma is excited to welcome the 2020 cohort of students who will embark on achieving Postgraduate Qualifications in Good Manufacturing Practice (GMP) from the University of Technology Sydney. The cohort represent a mix of graduates and working professionals from around the world, some of whom will undertake these studies on-campus in Sydney,...

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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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SeerPharma to Sponsor 8th Annual BioMelbourne Device + Diagnostics Lab

February 03, 2020

SeerPharma is excited to be sponsoring BioMelbourne Network’s 8th Annual Device + Diagnostics Lab, to be held on Thursday the 5th of March.

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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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Comprehensive On-Site GMP Training for Pharmaceutical Manufacturer

December 20, 2019

SeerPharma’s training division grows from strength to strength with several companies requesting tailored on-site QA/GMP training for staff. Recently a major multinational pharmaceutical manufacturer approached SeerPharma to address the following key areas of interest for staff at their firm:

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Following the GMP Opportunities Wherever They Lead

December 16, 2019

This article was originally published by the UTS Graduate School of Health is republished here with their permission.

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CSV Assistance for Pharmaceutical and Medical Device Companies

December 09, 2019

Several pharmaceutical and medical device manufacturers in the Asia-Pacific region have approached and engaged SeerPharma for assistance on matters related to Computer System Validation (CSV). Typical requests have seen SeerPharma address computer systems validation approaches to meet the regulatory requirements of Annex 11 of the PIC/S Guide to...

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2019 ISPE South Asia Pharmaceutical Manufacturing Conference (India)

November 18, 2019

SeerPharma exhibited and attended the International Society for Pharmaceutical Engineering (ISPE) inaugural South Asia Pharmaceutical Manufacturing conference in Bangalore, India from 25 to 27 September 2019.

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Meet Online Graduate Certificate in GMP Student Esther Kopp

September 09, 2019

This article was originally published by the UTS Graduate School of Health is republished here with their permission.

Esther Kopp is a Manufacturing Pharmacist and one of our new online students from our Graduate Certificate in Good Manufacturing Practice (GMP) cohort.

Designed for professionals, the online course is suitable for those looking to...

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CSV Review of Applications & Practices for Pharmaceutical Manufacturer

August 26, 2019

A Pharmaceutical manufacturer has requested that SeerPharma conduct a Computer System Validation (CSV) review of their level of Good Manufacturing Practice (GMP) compliance around the activities and functions of their IT department. The CSV review will help provide confidence that their computerised system are in a Validated state.

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