News
EU Clinical Trials Regulation
Published: 2/2/2022
European Union pharmaceutical legislation known as the Clinical Trials Regulation
Pharmacovigilance Requirements for UK Authorized Products
Published: 5/2/2021
MHRA webinars regarding PV requirements for UK authorized products after Bexit
Remote Pharmacovigilance Inspections of MAHs During Pandemic
Published: 2/12/2020
Regulatory and procedural guideline and points to consider
Regulatory expectations from MAHs during COVID-19
Published: 24/9/2020
Q&A about regulatory expectations for medicinal products for human use during the COVID19 pandemic.
MHRA post-transition period information
Published: 24/9/2020
More Information and guidance concerning MHRA post-transition period for industries and organisations.
Registering new packaging information for medicines in UK
Published: 8/9/2020
New guideline for registering new packaging information for medicines in UK from 1 January, 2021 and update on UK QPPV plus PSMF.
On-site GxP Inspection Programme
Published: 28/8/2020
Guidance for industry on MHRA's expectations for return to UK on-site inspections
Nitrosamine Impurities
Published: 28/8/2020
Marketing Authorisation Holders' submission of nitrosamine risk evaluation
Guidance for medicine developers and companies on COVID-19
Published: 29/6/2020
EMA encourages medicine developers and pharmaceutical companies who are working on medications and vaccines in regard to COVID-19
Stakeholders: Regulatory expectations during COVID-19 pandemic
Published: 29/6/2020
How COVID-19 is affecting my GMP/GDP licence when renewal is approaching
EMA recommended granting conditional MA to Remdesivir
Published: 29/6/2020
Seems that first approved COVID treatment will go through registration
Brexit in pharma
Published: 4/10/2018
EMA and MHRA published Brexit Preparedness Business Continuity Plan, ready to address all challenges for your business
EUPV essential and challenges
Published: 4/10/2018
Fom pharmacovigilance contracts to daily routine PV activities with obligation reports .
Ready for pharmacovigilance inspection
Published: 4/10/2018
USFDA recent campaign of focus PV inspection in Asia, main challenges in social media.
Serialisation
Published: 4/10/2018
Driving business value from pharmaceutical serialisation, challenges you will be facing – strategic advice as well as pragmatic solution
NEW entry to OTC
Published: 10/8/2018
Pharmazet Group is pleased to registration of first set of own products in OTC range as per our plans to enter to OTC market within CEE region.
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