|
|
|
| Prove A Sterility Assurance Level Of 10⁻⁶ | Article | By Kurt McCauley and Laurent Berliet, Mesa Laboratories | Explore the Biological Indicator/Bioburden (BI/BB) method for achieving sterilization of products along with the prerequisite studies needed to develop the sterilization process. |
|
|
| A Practical Road Map For EU GMP Annex 1 Compliance | Webinar | Lighthouse Instruments | Learn how to interpret the Annex 1 container closure requirements, develop deterministic analytical methods for CCIT, and design packaging studies that generate robust data demonstrating good CCI. |
|
|
|
|
| Elevating Quality Beyond Compliance | Article | By Mike Jovanis, Veeva | See how one company was able to connect its quality processes, improve collaboration across business functions, and address the needs of its digitally-aware workforce. |
|
|
|
|
|
| Key Considerations When Filling Dual Chamber Syringes | White Paper | By Giel van Veen, Dec Group | Dual-chamber syringes (DCSs) are in high demand across the pharmaceutical and hospital industries. Gain insight into the challenges of the DCS filling manufacturing market and how to overcome them. |
|
|
| Solutions For Accelerated Pharmaceutical Development | Article | By David K. Lyon, Ph.D., and Conrad Roten, Ph.D., Lonza | Explore an integrated service package designed to simplify and accelerate the development pathway, even for APIs with challenging properties such as low aqueous solubility and poor bioavailability. |
|
|
|
|
By Paul Allen, Clarkston Consulting | Deploying a laboratory information management system (LIMS) can boost your quality control lab's productivity, but how are you going about it? This article shares key steps and considerations for setting up your physical lab, controlling inventory, and more. |
|
|
|
|
|
|
|
|
Connect With Pharmaceutical Online: |
|
|
|