Legal & Regulatory

Academic study finds evidence of an early warning system in anonymized Web searches

Recent regulatory actions and court cases highlight the importance of due diligence in reporting the value of service fees when federal reimbursements are concerned. The financial consequences can be substantial

Number of cases opened by FDA's Office of Criminal Investigations (OCI) triples to 170

As the business grows at double-digit rates, representing its interests becomes its own business opportunity

A new policy debate over drug regulation is emerging as the NECC scandal worsens

As the number of adverse events (AEs) grows year by year, regulators and industry managers are looking at automated systems to handle the burden

Pricing systems in US drug supply chain have many limitations; an analytics-based method might avoid some of them

New incentives for health plans could alter the way payers review new drugs

As payers seek higher-quality data from real-world treatment settings, the importance of reliable measures becomes critical

New sample reporting requirements will be a focus of this year's meeting

Despite the lack of headlines today as compared to late last year, the drug-shortage situation has not improved. FDA, congressional and industry actions are beginning to change the dynamic

The pioneering firms that installed serialization and track-and-trace systems are being joined by a fast follower crowd, but an industry-wide commitment is still in the future

The 'Sunshine Act' provisions of the Affordable Care Act require records to be kept beginning Jan. 1

A combination of regulatory processes and business practices are worsening an already-bad drug shortage situation

Google and other web search engines have already tightened their controls for online pharmacy advertising; now they know the penalty for not doing so

The industry is far from ready when it comes to collecting, aggregating, cleansing and disclosing data about regulated financial transactions with doctors and hospitals

First-ever study of the impact of REMS on supply chains finds that collaboration is a critical requirement

Caseload reinforces concerns over illegal trade and distribution of pharmaceuticals

Industry and regulators are taking steps to revolutionize the basic regulatory function of collecting and analyzing adverse medical events

More pieces for industry-wide track-and-trace are falling into place, but there’s no rush to authenticate products

Senator Michael Bennet wants better FDA oversight of drug supply chain and material sourcing, as survey shows that 36% of Americans likely to vote have heard of unsafe ingredients

A Process-Based Assessment (PBA) is the first step to analyzing reporting needs

REMS programs need to address stakeholder usability