The Vaccine for COVID19: What kind of vaccines are

The most important epidemic of this century has affected the entire planet and has shaken our economic and social system. To face this common enemy, resistance was organized around the scientific community. A new hope is on the horizon so that we can return to our former lives, a vaccine that would allow us to be protected and no longer fear being infected or infecting our family, friends, or colleagues. We already have the weapons and the knowledge to develop a vaccine against COVID19 so that we can get back to the life we had before.

The Vaccine for COVID19: Your Immune System At

The immune system is one of the most successful mechanisms of human evolution. Globally, the immune system is ready to go to war, and the word is not too weak as it fights against anything that does not belong to our body, like the Coronavirus. So, how does it work?

How to prepare for Computer Software Assurance – Webinar

Working towards GMP? Learn which of your computer systems require validation, which do not, how to implement this process successfully, and the key deliverables according to GAMP-5. In this webinar we will focus on the question: How to prepare for Computer Software Assurance?

Project Management Tools in the Pharmaceutical Industry

This article focuses Project Management Tools in the Pharmaceutical Industry and shares insight into their use. The goal is not to provide a full detailed tutorial for each tool but to show their purpose and good practices for their use. And, don’t forget to download our set of free Project Management Tools here.

How To Design An Aseptic Processing Isolator

This article focuses on using the 6M tool as a support of the design of an aseptic isolator. The objective is to provide a generic assessment of the machine requirements to ensure that all key aspects are taken into account, and common mistakes are avoided. Thus answering the question: How to design an aseptic processing isolator using 6M?

Download our free GxP compliance checklist!

Do you want to assess whether your organisation is meeting GxP requirements? Use the below checklist and find out whether GxP fundamentals are well-established in your business and where you can still improve.

Checklist: Transitioning from CSV to CSA

If you are starting your preparation, aim to be proactive and develop a strategy on how to transition your current CSV framework to a CSA and focus on quality assurance, patient and product safety, and data integrity.

What Are Qualification And Validation

Qualification and validation are two words we use a lot in GMP, and sometimes we interchange them. This blog explains the difference between these two terms and introduces how qualification and validation help ensure compliance in the pharmaceutical industry.

pi joins Abylsen Group & unveiling a new identity

For 18 years, pi Life Sciences has been a global integrator of excellence for the world’s leading life sciences companies. pi Life Sciences joined the Abylsen Group in 2018 to mutually strengthen our business expertise and thus have a synergy between the two entities. pi offers unique expertise with the highest quality strategic advice, Abylsen […]