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Theoretical vs Tactical Good Manufacturing Practices Lunch and Learn

November 25, 2020

15 December 2020 | 12:00 p.m. AEDT

It’s vital to follow the latest good manufacturing practices. But what are the most efficient and effective ways to put GMP theories into action on your shop floor? Join MasterControl’s Ciaran O'Keeffe and Luana Carone as they welcome David Spaulding and Rohan Bhatia from SeerPharma for this free lunch and...

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Master of GMP Now Online | Online Information Session 16-Nov-2020

November 04, 2020

SeerPharma has partnered with the Graduate School of Health at the University of Technology Sydney (UTS) to deliver postgraduate qualifications in Good Manufacturing Practice (GMP). SeerPharma and UTS have worked tirelessly in the background to migrate this course for online delivery over the last few years to provide working professionals the...

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SeerPharma Sponsoring BioSymposium : COVID-19 Global Progress Update

October 26, 2020

BioMelbourne Network is an industry-led membership association for organisations engaged in biotechnology, medical technology and health innovation in the state of Victoria, Australia. BioMelbourne Network plays a pivotal role in fostering links between companies, research organisations, financial markets and government in Australia’s largest...

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MasterControl Launch Manufacturing Excellence for the APAC Region

October 20, 2020

With cloud infrastructure now in place in Australia, Singapore, Japan, China and India through Amazon Web Services (AWS), MasterControl have launched their latest Manufacturing Software Solution – Manufacturing Excellence (Mx) to the Asia-Pacific market.

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Vertex Pharmaceuticals Selects SeerPharma GMP eLearning for Global Use

October 06, 2020

Vertex Pharmaceuticals, Inc. is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. Vertex has multiple approved medicines that treat the underlying cause of cystic fibrosis (CF) — a rare, life-threatening genetic disease — and several ongoing clinical and...

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Computer Software Assurance - Configuration, Design & Closing the Loop

September 30, 2020

In the previous article, we looked at including Test Cases and the Functional Risk Assessment into the Functional Requirements Specification. This provided multiple benefits over maintaining these as separate documents:

  • Forces requirements to be testable (described in the test cases)
  • Forces thinking using ‘what if’ scenarios on requirements which...
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2020 PDA APAC Pharmaceutical Manufacturing & Quality Conference

September 15, 2020

The Parenteral Drug Association (PDA) is the leading global provider of science, technology and regulatory information and education for the pharmaceutical and biopharmaceutical community. Founded in 1946 as a non-profit organization, PDA is committed to developing scientifically sound, practical technical information and resources to advance...

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Overview of ISO 13485 – Medical Device QMS Requirements

September 09, 2020

This article was originally published by SeerPharma's business partner MasterControl and is republished here with their permission.

Some medical devices are as complex as a remote, personalized heart failure sensor. Others are as simple as a tongue depressor. But all medical devices have one thing in common: they benefit immensely from being...

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Good Manufacturing Practice Online Information Session: 28-Sep-2020

September 07, 2020

SeerPharma’s core mission is to advance Quality and GMP-Best Practices for the Pharmaceutical and Medical Device sector. To help us achieve this goal, we partner with the University of Technology Sydney’s Graduate School of Health to offer Postgraduate qualifications in GMP. Pharmaceutical and Medical Device manufacturing are essential industries,...

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Meet Online Postgraduate GMP Student - Teresa Domagala

September 01, 2020

Teresa Domagala is the Director of Manufacturing Development in Innovative Biologics with a multinational pharmaceutical organisation. In her current role, Teresa overseas a team of scientists responsible for assessing the developability of therapeutic candidates and subsequently isolating and characterising cell lines for their expression.Teresa...

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