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- PMLiVE

clinical trial regulation

- PMLiVE

EFPIA looks to ABPI for comms director

Andrew Powrie-Smith will join EU pharma trade body in New Year

- PMLiVE

US proposes tighter rules on clinical trial reporting

If approved, data from around 650 additional studies per year will be released

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EU watchdog raps EMA for redacted AbbVie data

Issues over the redaction of clinical study reports

- PMLiVE

EFPIA promotes pharma’s contribution to Europe

Launches Pharmafigures website to detail industry investment

- PMLiVE

EMA draws fire on new clinical reports policy

Has recently come under pressure from transparency groups

- PMLiVE

The price is right: drug reimbursement in Europe

EFPIA's director general argues that drug pricing is not a gameshow

European Commissioner for health and food safety elected

Vytenis Andriukaitis will take on the role from October

National Institute for Health and Care Excellence NICE logo

NICE wants greater access to clinical data

Will turn to European regulators if companies fail to provide information

- PMLiVE

Pharmaceutical doctors want all trial data published

Faculty of Pharmaceutical Medicine shows support for greater clinical transparency

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International regulators collaborate on generics

EMA leads three-year pilot project to increase pre-market data sharing

- PMLiVE

UCB joins clinical trial data sharing portal

Follows GSK, Lilly, Roche and others in committing to transparency website

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EMA transparency policy delayed over ‘wording’

Regulation on access to trial data postponed until October

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