How To Evaluate Sterile Products For Package Integrity
Learn more about USP 1207 guidelines and how to evaluate package integrity for sterile products in pharmaceutical industry.
Learn more about USP 1207 guidelines and how to evaluate package integrity for sterile products in pharmaceutical industry.
Learn more about different categories for packaging quality requirements for medical devices, pharmaceutical products, and multi-dose products.
Learn more about the USP 51 requirements for preservative challenge testing for your medical products.
What is preservative efficacy testing? Learn more about preservative efficacy testing (PET) and its importance for regulatory approval of your product.
Learn about package integrity testing and evaluation, differences with container-closure integrity, leak testing, seal quality testing, and more.
Learn about seal strength testing for product packaging, its techniques, standard modes of failure, why it is important and how it is performed.
Learn about bubble emission testing for porous packaging materials, test methods, and its importance in ensuring the integrity of your medical device packaging.
Learn all about stability testing, what is accelerated aging, why accelerated aging is used, and how accelerated aging testing is performed.
Learn about dye penetration testing for porous packaging materials, test methods, and its importance in ensuring the integrity of your medical device packaging.
How do you choose the best contract manufacturing partner? Learn more about some mistakes you can fall into as a Start-up.