Whether they are building a new healthcare IT system from scratch or a groundbreaking medical device, many biotech and life science startups need easy-to-use tools specifically designed to help streamline agile projects and/or manage the entire software lifecycle.
Advanced Therapies Meeting FemTech: Focus on the Prenatal and Perinatal Diseases
Stop Checking The Box: Leveraging Your Employer Brand To Enhance Your DEI Initiatives
Immediately Better Hiring: 9 Things to Do Right Now Guest Post by James Ellis, Principal of Employer Brand LabsJune 12, 2023 Want to hire better? Of course you do. Your [….]
Failure Mode and Effects Analysis (FMEA) – a General Overview Guest Post by Daniela Siu Manzano and Dante Amatangelo, PQE GroupMay 23, 2023 All biopharmaceutical companies in the process of [….]
What’s Your Strategy for Attracting and Hiring New Grads? Guest Post by James Ellis, Principal of Employer Brand LabsMay 23, 2023 Tis the season of new grads. And while your [….]
Commissioning and Qualification of Laboratory Instruments Guest Post by PQE GroupApril 28, 2023 Commissioning and Qualification of a laboratory instrument is the documented collection of activities that are delivered within [….]
Biotech Startups Have No Excuse to Ignore Employer Brand Guest Post by James Ellis, Principal of Employer Brand LabsApril 17, 2023 Biotech startups are defined by two things. First, by [….]
In the pharma/biotech space, talent generally gets to choose where they want to work. But in order to make an informed choice, they require specific, differentiated information about potential employers and what kind of culture, values, and working experience they can expect.
Manual visual inspections include everything from filling the product, inspecting it, and acceptance sampling (AQL), which means a certain amount of product is scrutinized at a higher level. If a certain percentage of the total amount being tested shows defects, the entire batch must be addressed. Continuing education following training is important; industry trends are moving so quickly, and adapting so dramatically, it is challenging to keep up with these regulatory guidances, which are revised and updated periodically. The responsibility is on the manufacturer. Just a few examples of FDA’s guidance with respect to manual visual inspections include:
