Discover the essential features of radiopharmaceuticals production in this informative blog post.
Learn about SPOR (Substance, Product, Organization and Referential), the European Medicines Agency's requirement for implementing ISO IDMP standards..
Gain insight into the challenges faced by early-stage life science startups and discover what it takes to succeed in the competitive business.
Commissioning and qualification are vital phases in the validation process of the pharmaceutical industry. Learn how these phases ensure quality and.
Discover the potential future applications of CBD in veterinary medicine, including its use as an analgesic, antiepileptic, and treatment for.
Discover the importance of accurate alarm assessment documents in ensuring a proper alarm management process in pharmaceutical manufacturing. Learn.
Discover the current state of AI and the governmental initiatives being taken to address associated risks. Learn about the recent AI Act and.
Discover how PQE Group empowers customers during the software selection process. Overcome challenges, maximize effectiveness, and ensure project.
Learn how to manage regulatory assessments for clinical trials for medical devices and medicinal products. Understand different scenarios and.
Discover the process of medical cannabis registration in Italy and the requirements for obtaining a cultivation license.