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The Canadian Regulatory System for Cell and Gene Therapies
Understanding the Role of the Quality Unit in Good Manufacturing Practices
Viral Aggregation in Downstream Processing of Lentiviral Vectors
Planning Is Everything - Quality Control Testing in Cell and Gene Therapy
What Are Change Controls and Why Are They Important in GMP?
21 Sep 2022

Top 3 Trends in Cell and Gene Therapy

Thanks in part to lessons learned and trends accelerated by COVID-19, ...

05 Jul 2022

Scaling-up Versus Scaling-out: Here’s What You Need To Know

A lot of CDMO customers ask about scale-out and scale-up, and what app...

08 Dec 2021

What Are Change Controls and Why Are They Important in GMP?

Good Manufacturing Practices (GMP) are built on documentation. A commo...

03 Aug 2021

CCRM Collaborates To Tighten Timelines and Prepare Nkarta for IND Filing

CCRM works with customers in a collaborative manner to enable them to ...

27 Jul 2021

3 Ways Your CDMO Can Help You Avoid Supply Chain Problems

The COVID-19 pandemic has significantly disrupted supply chains and pr...

12 May 2021

How CCRM's Unique Approach Enables Client Success

Outsourcing to a contract development and manufacturing organization (...

01 Dec 2020

3 Considerations When Developing Your LVV Program

If you are looking to get a lentiviral vector (LVV) program off the gr...

12 Aug 2020

CDMOs: The Good, the Great and the Exceptional (and How to Tell the Difference)

Outsourcing to a contract development and manufacturing organization (...

17 Apr 2020

Quality-by-Design Approach to Manufacturing Cell and Gene Therapies

Implementation of a manufacturing process that assures a predefined qu...

27 Mar 2020

Essentials of Auditing in the Manufacturing of Cell and Gene Therapies

Our previous posts on quality management systems and steps to ensure y...

13 Feb 2020

Understanding Cryopreservation of Cellular Therapies

Cryopreservation is the process of using ultra-low temperatures to pre...

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