It Takes a Bio/Pharma Village
Precompetitive efforts of the members of the IQ Consortium have demonstrated that collaboration from a global bio/pharma village is essential to serve patients.
The proverb “it takes a village to raise a child” illustrates the importance of community involvement to help children develop in a safe environment. In the bio/pharmaceutical industry, researchers nurture new drugs through the development and manufacturing process internally or with support from external contractors and suppliers. Major science, technology, and regulatory challenges, however, require collaborative efforts from across the industry.
Precompetitive research efforts between academia and industry have spurred innovations in analytical science and manufacturing. And efforts by expert industry volunteers—with the support of bio/pharmaceutical companies—have tackled, and continue to address, some of the pressing technical, scientific, and regulatory issues facing all drug companies.
The following special section of this Regulatory Sourcebook, Quality Collaboration, features contributions from members of the International Consortium for Innovation & Quality in Pharmaceutical Development (IQ Consortium). The not-for-profit organization of pharmaceutical and biotechnology companies works collaboratively to develop solutions to common problems on a precompetitive basis.
Through case studies and reports on working group activities, the authors share examples of how these organized collaborations can improve research and development efficiency, mitigate risks, and improve quality, while sharing costs for addressing scientific, technical, and regulatory questions.
This section highlights the efforts of IQ Consortium working groups to address pharmacokinetic modeling, safe handling of biologic drugs by healthcare workers, phase-appropriate specifications for biologic drugs, extrapolating adult clinical trial data for pediatric studies, data integrity, and good laboratory practices.
Other Consortium initiatives, not discussed here, address analytical practices, drug substance and drug product, good manufacturing practices, continuous manufacturing, dissolution, novel excipients, process analytical technology, accelerated drug development, and more.
For more than a decade, the efforts of the members of the IQ Consortium have demonstrated that collaboration from a global bio/pharma village is essential to serve patients.
Read this article in BioPharm International's Regulatory Sourcebook March 2021 eBook.
Article Details
BioPharm International
eBook: Regulatory Sourcebook
March 2021
Page: 22
Citation
When referring to this article, please cite it as BioPharm International, "It Takes a Bio/Pharma Village," BioPharm International Regulatory Sourcebook eBook (March 2021).
Regeneron Treatment for Multiple Myeloma Gets Conditional Marketing Approval from EC
April 29th 2025The indication is specific to patients who have received at least three prior therapies, including a proteasome inhibitor, immunomodulatory agent, and anti-CD38 monoclonal antibody, and have demonstrated disease progression on the last therapy.
MHRA Approves GSK Therapy Combinations for Multiple Myeloma
April 21st 2025Belantamab mafodotin is approved in combination with bortezomib plus dexamethasone in patients who have had at least one prior therapy, and in combination with pomalidomide plus dexamethasone for those who have had a prior therapy including lenalidomide.
