Medical Writing: From Protocol to Publication

Your AMS team of dedicated medical writers will assist you with the creation of all required documents from protocol to publication.

Medicalwriting bottom

• 2021 – New Literature Search tool launched • 2021 – DIGA dossier submission pioneer • 2021 – NIS-eTMF launched • 2021 – MDR readiness, AMS prepared for Medical Device Trials under new regulation • 2021 – VO (EU) 536/2014, AMS among the first 100 participants in the EMA CTIS Trainer Programme • 2021 – eSignature, AMS introduced DocuSign® • 2017 – Globally unique AMS-ePRO® features • 2016 – CRO of the year award •

News

Donation: AMS contributed Laptops for...

Informationen
Artikel vom 29 Juni 2022 News

Donation: AMS handed 15 Laptops over for Pupils from Ukraine School Homepage in German: https://www.lfg-ma.de/2022/05/31/ams-spendet-15-laptops/

Read More
Accreditation from the French Research...

Informationen
Artikel vom 07 Juni 2022 News

For our Customers in France: Accreditation from the French Research Ministry within the framework of Research Tax Credit (Crédit Impôt Recherche - CIR) AMS...

Read More
European HTA Webinar

Informationen
Artikel vom 30 März 2022 News

European HTA - What have we learned, what lies ahead? Free Webinar on 4th of May 2022 Join us as we share our experiences and learnings fromEUnetHTA Joint...

Read More
European Union's New HTA Regulation

Informationen
Artikel vom 18 Februar 2022 News

European Union's New HTA Regulation entered into force on 11 January 2022 and will apply on 12 January 2025. However, its implementation starts now and will...

Read More
Webinar: Real World Data - New...

Informationen
Artikel vom 31 Januar 2022 News

FEB 24 2022 Webinar: Real World Data New Frontiers in the RWD and Current Use-Cases for RWD Collection Powered by AMS and Glatt Pharmaceutical Services Fewer than...

Read More
Regulatory Update - New Cooperation

Informationen
Artikel vom 27 Januar 2022 News

Online Course: Update Medical Device Regulation AMS developed together with KKS Heidelberg, Department for Advanced Training and Metecon GmbHDepartment for...

Read More
CTR and the CTIS - Clinical Trials...

Informationen
Artikel vom 28 Oktober 2021 News

CTR and the CTIS - Clinical Trials Information System The Clinical Trial Regulation (CTR) will come into force on 01 Feb 2022. The CTIS submission platform...

Read More
EU HTA – Health Technology Assessment...

Informationen
Artikel vom 21 Mai 2021 News

EU HTA – Health Technology Assessment across Europe How to bridge the gap between EUnetHTA's cessation and an EU Regulation's application? Considering the fact that EUnetHTA...

Read More
10 Jahre AMNOG - Rückblick und Ausblick

Informationen
Artikel vom 26 April 2021 News

10 Jahre AMNOG - Rückblick und Ausblick Dieses Jahr wird das 10-jährige Bestehen des Arzneimittelmarkt-Neuordnungs-Gesetzes AMNOG gefeiert. Als Dienstleister der ersten...

Read More
EUnetHTA Open Call for Early Dialogue...

Informationen
Artikel vom 09 Juli 2020 News

EUnetHTA’s Joint Action 3 has been prolonged to May 31, 2021. After a temporary suspension of Early Dialogues (ED) due to the current pandemic situation, ED...

Read More
EMA-EUnetHTA Parallel Consultation

Informationen
Artikel vom 01 August 2017 News

Profit from the simultaneous feedback of regulatory and HTA bodies in order to generate your data set in the most efficient way! What is new? EMA and EUnetHTA have...

Read More
AbbVie TRIUMPH AWARD 2015

Informationen
Artikel vom 24 Juni 2016 News

Um Kooperationen auszuzeichnen und Partner entsprechend zu honorieren, verleiht AbbVie Global jährlich den Preis 'Supplier of the Year'. Kriterien, um für den...

Read More
AMS electronic Patient Reported...

Informationen
Artikel vom 01 Juni 2016 News

AMS electronic Patient Reported Outcomes (AMS-ePRO®) AMS-ePRO® supports Clinical Research You can now capture your patients data Anytime Anywhere with...

Read More