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viable cell density

Open timbrisc opened this issue 2 years ago • 7 comments

Issue migrated from trac ticket # 5826

component: organization | priority: minor | keywords: VCD

2022-06-07 21:09:51: [email protected] created the issue


UCUM Board needs to provide input. UCUM already has mass density, linear mass density, lum. intensity density, magnetic flux density, and spectral density, so adding a UCUM term called "viable cell density" would be somewhat consistent. Viable cell density is the number of living cells per unit volume. Please see http://www.oilgae.com/ref/glos/cell_density.html.

This new concept is needed to support the U.S. Food and Drug Administration Pharmaceutical Quality Chemistry Manufacturing and Control (PQ/CMC) initiative. Please see https://www.regulations.gov/document/FDA-2022-N-0297-0001, which in part, states:

"PQ/CMC is a term used to describe manufacturing and testing data of pharmaceutical products. PQ/CMC encompasses topics such as drug stability, quality specification, batch formula, and batch analysis, which are important aspects of drug development. PQ/CMC plays an integral part in the regulatory review process and life cycle management of pharmaceutical products. The development of a structured format for PQ/CMC data will enable consistency in the content and format of PQ/CMC data submitted, thus providing a harmonized language for submission content, allowing reviewers to query the data, and, in general, contributing to a more efficient and effective regulatory decision-making process by creating a standardized data dictionary.

The impetus for this standardization effort was the provisions from the 2012 Food and Drug Administration Safety and Innovation Act (Pub. L. 112-144), which authorized the Agency to require certain submissions to be submitted in a specified electronic format. PQ/CMC standardization supports FDA's regulatory needs in receiving structured and standardized data in pharmaceutical quality and includes two objectives: (1) To standardize the pharmaceutical quality data that is currently received by FDA in eCTD Module 3 from the sponsoring organizations, and (2) to use these structured elements and develop a FHIR data exchange solution."

timbrisc avatar Jun 07 '22 21:06 timbrisc