European experience to date indicates a changing perspective on biosimilar pricing
Longitudinal patient-level data answer pressing questions about patient safety, outcomes and medication acceptance
In this Pharmaceutical Commerce video interview, Joerg Tritschler, a partner in Simon-Kucher’s life sciences division, explores the two major strategies big pharma companies are employing amid current macro challenges and efforts to offset looming patent losses to blockbuster brands.
Digital systems are changing the economics and functionality of scheduling and production of printed packaging
Industry and FDA can—and must—do more to protect global pharmaceutical supply chains
‘Class of Trade’ is a murky element of contracts and channel analytics that can have important legal implications
How they embrace collaboration will be key to the battle against RSV.
The current economic downturn may fuel the creation of new, more sustainable business models
Usually associated with manufacturing or laboratory processes, quality systems can improve post-marketing compliance efforts
In the race to improve product performance, not enough attention is paid to 'who's actually going to switch?'
A Process-Based Assessment (PBA) is the first step to analyzing reporting needs
Vaccine administration is shifting from multidose vials to prefilled syringes for a host of important safety and economic considerations
While FDA guidance on appropriate medical communication has evolved, US Dept. of Justice attention the practice is intensifying
Go-to safeguards for manufacturers in avoiding mismanagement of their business-central records
An inside look at selection and implementation of passive thermal protection
Pharma marketers become adept at refining coupon and voucher programs, while technology options multiply. Meanwhile payer criticism mounts
The National Council for Prescription Drug Programs’ (NCPDP) Billing Unit Standard (BUS) brings order to pharmaceutical transactions. Between it, the National Drug Code (NDC) and the Structured Product Label (SPL), all necessary commercial information about a product is known.
The Medical Affairs function can play a vital role in today’s product launch process
Big Data and AI will bring value beyond compliance
Under the theme of personalized medicine, in vitro diagnostics will play an increasingly important role in new drug entries and new therapies
Patient-support Hub services are a vital repository of the patient journey
Cloud computing opens a new array of benefits--and challenges--to data-sharing
As payers seek higher-quality data from real-world treatment settings, the importance of reliable measures becomes critical
Drug sponsors have options in both how the new FDA risk programs are structured and how to execute them
Industry response may be to keep more innovations as trade secrets
Data from prior Phase II study showed signs of pridopidine slowing disease progression in patients with amyotrophic lateral sclerosis.