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Latest articles2018-04-20T09:26:06+00:00

Who is responsible for employee activities on SoMe?

Updated guidelines on the promotion of medicinal products The Danish guidelines on company responsibility for employee activities on social media have been updated to be more specific and a comprehensive list of questions [...]

By |mar 6th, 2018|Categories: All, Marketing Support|Tags: |

Strengthened knowledge regarding promotion of medicinal products

Well-documented knowledge is a core driver for PharmAdvice. It enables us to provide high-quality service and professional advice to our customers We have strengthened our knowledge regarding promotion of medicinal products and are [...]

By |nov 14th, 2017|Categories: All, Marketing Support|Tags: , |

New safety advice for excipients demands improved labelling information

New safety advice for excipients demands improved labelling information The European Medicines Agency (EMA) and the European Commission have updated the annex to the European Commission’s guideline on ’Excipients in the label and [...]

By |okt 24th, 2017|Categories: All, Marketing Support, Pharmacovigilance (PA)|Tags: , , |

New Risk Management Plan (RMP) template becomes mandatory

The new Risk Management Plan format – a major improvement for generic and well-established products By Ea Dige On 30 March 2017 EMA published Revision 2 of the guidance on the format [...]

By |sep 22nd, 2017|Categories: All, Pharmacovigilance (PA)|Tags: , |

Company responsibility for employee SoMe activities

New Danish guidelines include company responsibility for employee activities on the social media According to an updated version of Danish guidelines on digital medias for promotion of medicinal products, companies may now be [...]

By |sep 18th, 2017|Categories: All, Marketing Support|Tags: , |

Strengthened team of Regulatory Affairs professionals

Extended resources strengthen our team of Regulatory Affairs professionals We are pleased to announce that Sonja Horsted, MSc. Pharm, has joined the Regulatory Affairs team at PharmAdvice on June 1, 2017. Sonja has [...]

By |jul 29th, 2017|Categories: All, Regulatory Affairs (RA)|Tags: |

Good practice for documentation of safety variations

How to ensure good practices for documentation of safety variations By Ea Dige Ensuring good practices for documentation and management of safety variations, starts by optimizing the cooperation between your Regulatory Affairs [...]

By |apr 28th, 2017|Categories: All, Pharmacovigilance (PA), Regulatory Affairs (RA)|Tags: , , |