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4 days ago · In 2011, the FDA introduced guidance on the process validation life cycle, including continued process verification (CPV).1 While implementation is becoming a regulatory expectation, CPV can provide benefits beyond compliance by identifying opportunities to improve production processes and ultimately, the reliability of drug quality and supply.
I can't think of any laws against not posting roles internally or externally. While it may not be best practice for a number of reasons, and could indicate other concerns, it is unlikely illegal. Yes, it’s legal and could be a good business practice if they are able to snatch up good talent quickly.
3 days ago · Community pharmacy professionals (CPPs) play an important role in the healthcare system, have a greater impact on public health programs, and play a critical role in patient education. 3 Because of their ease of accessibility, lack of need for an appointment to interact with patients, and widespread geographical distribution, CPPs seem to be ideally positioned to implement health prevention ...
3 days ago · The data should be quantitative rather than qualitative. Numbers and scope will matter. When you score a meeting with district personnel, you’ll likely present to the senior administration team. Your presentation should be polished and professional. Provide handouts and real-time demos if possible.
At the moment you have minimal product descriptions. I would recommend better images and removing countdown timers (They appear a little cheap and people know they're fake) and going for a more high end pet store to differentiate yourself from the big players I mentioned before. I have some examples of pet stores that are killing it if you want.
4 days ago · A fundamental GMP requirement is that processes, systems, and methods used to produce medicines and treatments are validated, meaning their fitness for a purpose is demonstrated. If Industry 4.0 is to succeed in the pharma space as Pharma 4.0™, we need new paradigms for validation across the value chain that use new technologies to improve product quality and the safety of medicines and ...
2 days ago · Process analytical technology (PAT) is perceived as the main enabler for a robust control strategy with continuous manufacturing (CM) because process analytical technology can aid in implementing continuous manufacturing throughout the entire life cycle. This article discusses quality and regulatory hurdles in the life cycle of a process analytical technology application—including model life ...
