Welcome to
Dr. Notghi Contract Research
Clinical Trials | Submission | Pharmacovigilance
Your established CRO Partner since 1999 in the heart of Berlin
for safety in clinical trials and post-market surveillance
🇬🇧 German
More than a full-service CRO
Dr. Notghi Contract Research GmbH is your partner for holistic and high-quality project management around clinical trials, non-interventional study projects, drug safety and pharmacovigilance. Furthermore, together with our customers, we meet regulatory requirements for the publication of studies and study results.
As a full-service CRO, our interdisciplinary team of experienced scientists and doctors, together with our experts, offers reliable and efficient services in our environment. We maintain trusting relationships with our customers, employees and cooperation partners and form a strong network with them.
In addition, the Dr. Notghi Academy has been training specialists and executives for clinical research and pharmacovigilance for over 10 years. It also offers GCP courses for investigators and study staff and trains study nurses.
Clinical trials
You are planning to conduct a clinical trial with a medicinal product or a medical device in cooperation with an established CRO partner?
With 20 years of experience in conducting clinical trials in accordance with ICH-GCP and ISO 14155, the staff of Dr. Notghi Contract Research GmbH accompany and advise pharmaceutical companies and sponsors in the collection and evaluation of clinical data within the framework of clinical trials & studies for medicinal products and medical devices.
You need know-how and reliable services in drug safety and pharmacovigilance?
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For more than 15 years, the team of Dr. Notghi Contract Research GmbH has been an established service partner in pharmacovigilance and drug safety. We take over the timely processing and reporting of suspected and adverse drug reactions for our clients.
Furthermore, we undertake global and local literature searches, the preparation of periodic safety reports and risk management plans as well as the preparation and maintenance of your pharmacovigilance master file.
We are a reliable service partner for you both during the conduct of clinical trials and after approval. Benefit from our conscientious way of working.
Pharmacovigilance
Pharmacovigilance
You need know-how and reliable services in drug safety and pharmacovigilance?
For more than 15 years, the team of Dr. Notghi Contract Research GmbH has been an established service partner in pharmacovigilance and drug safety. We take over the timely processing and reporting of suspected and adverse drug reactions for our clients.
Furthermore, we undertake global and local literature searches, the preparation of periodic safety reports and risk management plans as well as the preparation and maintenance of your pharmacovigilance master file.
We are a reliable service partner for you both during the conduct of clinical trials and after approval. Benefit from our conscientious way of working.
Submission
As a sponsor, you are subject to the obligation of transparency in clinical trials, i.e. in the publication of Interventional, Non-Interventional and EU PAS studies.
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The Dr. Notghi Contract Research GmbH team focuses on the regulatory and legal obligations of sponsors to publish clinical (interventional), non-interventional and EU PAS studies in accordance with EU, US and German regulations.
We are your reliable partner
Our expertise
- 20 years in the conduct of clinical studies & trials
- 15 years in pharmacovigilance and drug safety
- 10 years in the publication of study data
Your advantages
- Reliable services
- Short communication channels
- Broad competence for complex projects
Working together
- Eye level & trust
- All-round view & forward thinking
- Discreet & direct
Do you have any questions about our services?
We are also happy to answer them personally.
