@dokumeds

Dokumeds.com

6 Tips for Managing Clinical Trial Logistics in Russia

5 Key Considerations for Planning Paediatric Clinical Trials in the EU

GDPR and Clinical Trials: Data Transfers within EEA (European Economic Area) and to Third Countries

How to Minimise Change Orders

Clinical Trials in Oncology - Key Points to Consider

Adapting to Cultural Differences to Positively Impact Clinical Trials

Pros and Cons to Working with a Mid-Size CRO

Increasing Clinical Trial Enrollment Through Innovative Digital Techniques

Tackling Risks Related to Unforeseen Project Costs

Medical Devices: Are You Ready For EU MDR 2017/745?

Emerging Increase in Medical Science Liaisons in Clinical Development

Clinical Trials in Ophthalmology

Scientific and Medical Expertise for Successful Clinical Development

COVID-19 Implications on Clinical Trial Site Auditing

Overcoming Challenges in Rare Disease Clinical Research

CRO Project Manager Retention as a Key Factor for Clinical Trial Success

E-BOOK: The Ultimate Guide to Pharmacovigilance in the EU

COVID-19 Impact – Enrollment in Clinical Trials

E-BOOK: Oncology Clinical Trials in Europe: Complete Guide

Employee Training Programs as a Quality Improvement Tool for Clinical Trials

Overcoming Risks to Clinical Trials during Pandemics

A Short Summary of the Regulations for Clinical Trials Across the EU – Upcoming Changes & Considerations

Defining the Request for Proposal (RFPs) Process for Clinical Trials

How to keep Clinical Trials on Budget

Outsourcing Tuberculosis Clinical Trials

Ensuring On-time Patient Recruitment in Clinical Trials

5 Ways Dokumeds Improved Study Start-up Times in Russia

The Importance of Finding New Vaccines and Drugs to Fight Tuberculosis

Dokumeds Passes GDP and ISO Surveillance Audits

E-BOOK: Paediatric Clinical Trials in the EU: How to Overcome Regulatory and Ethical Challenges

E-BOOK: Understanding the Supply Chain and Customs Regulations in Russia

The Importance of Scientific Advice from the Regulatory Authorities in Clinical Research

E-BOOK: A Roadmap to Navigate Regulations for Clinical Trials in the European Union

How to Successfully Outsource your Pharmacovigilance

WEBINAR: Accelerate your Trials with Efficient Enrolment

Dokumeds’ Expansion into South Africa

Dokumeds opens an office in South Africa

Discover Russia with Dokumeds: Regulatory Submission Overview in Clinical Trials

The Importance of CTA’s in the Clinical Research Process