Kinapse Contributes Comments to ICH Guideline Q12 :
An overview of comments received on guideline Q12 on technical and regulatory considerations for pharmaceutical product lifecycle management
Kinapse, a Syneos Health Company recognises guideline ICH Q12 as having the potential to completely change the regulatory post-approval landscape of the Pharma industry. Designed to complement existing Q8-Q11 guidelines to enable a full realization of more flexible regulatory approaches, the Q12 guideline relates to technical and regulatory considerations for pharmaceutical product lifecycle management.
On the 18th of January 2019, the European Medicines Agency published comments received during a public consultation of this draft guideline. Kinapse are proud to demonstrate our continued commitment to regulatory harmonization by having our comments included.
Follow the link below for more regarding guideline ICH Q12 and see below for Kinapse’ comment:
Kinapse’ General Comment:
“This is a good initiative; defining established conditions (ECs) for a drug product should minimize number of variations based on critical risk assessment and scientific approach.
The proposal (if adopted by a company) can pose a challenge for legacy products than newer products in terms of generating supplementary developmental studies for proposing ECs.
Both the Established conditions (ECs) and Product Lifecycle Management (PLCM) are the core of the Q12 guideline. Incompatibility of these concepts with the established legal framework is a matter of concern at the moment.”
To read more comments by Kinapse and other organisations:
Download white paper
Managing Performance in Patient Centricity:
Making the link between value for patients and value for the pharmaceutical industry