Healthcare discussions are booming on the Internet. How will FDA allow pharma to participate?
New IT data-science and visualization tools advance supply chain management
Not all managed care plans have the same influence on overall prescribing behavior, and not all geographies operate the same way
When entering the specialty pharmaceuticals arena, manufacturers need to evaluate the capabilities of their channel partners carefully
The longstanding adherence problem is yielding to new technology
Deep analysis of specialty pharmacy data shows opportunities for managing the patient journey
Varcode’s variable barcode records temperature and time out-of-compliance for pharma and perishables
Global efforts to collect clinical data in a more standardized form will lead to more research innovation
Compliance officers at pharma companies need to ensure that the right mechanisms are in place for monitoring sales and business incentives
Better local resources around the world and more sophisticated technology are changing the dynamics of logistics services
The SP channel continues to grow, with manufacturers looking for more control over access
A new, market-driven model of drug development and commercialization is appearing*
Retailers, distributors and manufacturers are being affected by federal rules on durable medical equipment (DME)
Personality assessments identify the traits that enable some pharma researchers to ascend to leadership roles in industry
Multiplying state laws on marketing and distribution disclosures might be pre-empted by new federal legislation
Marketing strategies will adjust with the advent of biosimilars
Applying the managed services model to commercial operations can result in dramatic savings as pharma companies globalize
Multiplying state laws on marketing and distribution disclosures might be pre-empted by new federal legislation
Converging the processes and data from EHRs and from the electronic data-capture (EDC) of the clinical research environment could change the paradigm of drug development and safety
Orphan drug development and marketing have important distinct requirements for R&D, regulatory and marketing
Risk Evaluation & Mitigation Strategy (REMS) programs are evolving, with new complexities for compliance managers
CLM Matrix system exploits Microsoft SharePoint platform
Nearly 30% of acquiring companies do not evaluate FCPA risks prior to an acquisition
Guidance for companies starting out on the commercialization path
What are the risks of future 'pay for delay' settlements between branded and generic manufacturers?