Ensuring Quality and Safety in the Pharmaceutical Industry
Pharmaceutical Standards are essential for ensuring the safety, efficacy, and quality of medicinal products and substances. Published by leading Standards Development Organizations (SDOs) like NSF, ISO, PDA, and ASTM, these Standards cover various aspects of pharmaceutical manufacturing and best practices, guiding organisations to maintain compliance and deliver high-quality products.
Key components include pharmaceutical primary Standards, which serve as benchmarks for active pharmaceutical ingredients (APIs), and pharmaceutical secondary Standards, utilised for quality control in laboratories. Compliance with pharmaceutical manufacturing Standards is critical, particularly regarding clean room Standards for pharmaceutical production, which minimize contamination risks in controlled environments.
Pharmaceutical Standard operating procedures (SOPs) foster consistency and reliability, facilitating effective training and adherence to best practices. Competency Standards define the necessary skills and attributes for practitioners, emphasising knowledge and experience in meeting pharmaceutical safety Standards.
Robust pharmaceutical Standards are crucial for protecting public health and fostering a culture of quality assurance within the industry. By prioritizing these Standards, the pharmaceutical sector can ensure the safe and effective delivery of medicinal products to patients worldwide.
Intertek Inform: Your source for Pharmaceutical Standards
Intertek Inform makes it easy for businesses to access pharmaceutical Standards from our website. Whether you need a single Standard or a tailored subscription, we provide flexible option to suit your needs.
You can purchase individual Standards in digital PDF or printed (hardcopy) formats through our user-friendly website. For more extensive needs, consider subscribing to i2i, our secure, cloud-based, configurable platform that allows for efficient management of Standards throughout your organisation.