Formulation Development

Pharmaceutical formulation development is the critical step which links the discovery of a novel drug to commercialization. During this step, formulation scientists will determine the best drug delivery vehicle and dosage form needed to deliver a therapeutic effect based on bioavailability or other factors. Below you can explore articles, industry trends, and curated products which can help increase formulation development efficiency.

Technology-Driven Innovation in Real World Evidence for Patient Registries
The demand for robust patient data and real-world evidence (RWE) continues to grow as regulators, payers, researchers, and physicians look to answer questions throughout the entire lifecycle of a drug. While patient registries are an important data source, traditional means of data collection greatly limit the types and amounts of information ... read more
Pre-Emptively Satisfying Agency Queries and Other Concrete Use Cases for Regulatory AI
Today, everyone has something to say about the potential for artificial intelligence – including Generative AI - in transforming Life Sciences companies’ use of regulatory data. But where could technology really play a role and deliver tangible everyday benefits? One emerging example is in searching and distilling insights from across companies’ ... read more

ebook: Lipid Excipients to Unlock Oral Bioavailability Issues
Oral dosage forms favor good patient acceptance and compliance in great part because they are easy to take. However, achieving sufficient bioavailability by the oral route can be challenging due to the complexity of the gastrointestinal (GI) tract. read more
Extractables and Leachables Research is Gaining Maturity
The pharmaceutical and medtech industries, along with their associated regulators, are paying increasing attention to testing requirements for extractables and leachables (E&L) to guarantee the safety, quality and efficacy of their products. read more
Manufacturing of Highly Potent APIs with Best-Practice Safety and Containment Control Procedures
It is a key regulatory and safety requirement that prospective hazards associated during the handling of HPAPIs are identified and understood to enable the development of Occupational Exposure Limits (OEL). read more
The NEXT GENERATION in Protein Characterization
The ability to measure and characterize changes in the secondary structure of proteins is critical to many research applications, especially the formulation and development of biotherapeutics. read more
Benefits of Using High-Functionality Excipients in a Continuous Manufacturing Process
As pharmaceutical companies move increasingly toward changing production methods from batch to continuous processing, there is a need to re-evaluate the types and formulations of the excipients used. read more