COVID-19 Implications on Clinical Trial Site Auditing
The COVID-19 pandemic has had unprecedented implications on clinical trials and research, ranging from...
The COVID-19 pandemic has had unprecedented implications on clinical trials and research, ranging from...
Rare diseases affect an estimated 3-6% of the global population, which may in fact be an underestimate...
Learn how to efficiently conduct your clinical study in Europe with our expert guide.
This e-book will provide you with key tips to successfully navigate pharmacovigilance for clinical trials in the EU
Russia, due to its vast population, availability of qualified investigators, and advanced diagnostic and treatment...
According to the European Medicines Administration (EMA), approximately 50% of all medications routinely used...
From a management perspective, clinical trials are complex operations: they involve multiple stakeholders...
The European Union (EU) provides important geographical coverage in clinical research...
The high biological variability involved in cancer and the stringent regulatory requirements make clinical trials...
Clinical trials is a multinational industry, where teams from different backgrounds come together to collaborate...
The complexity of running a clinical trial requires the involvement of various experts to ensure its success...
Once the planning and start-up procedures for a clinical trial are completed, the most critical part of the trial...
In today’s biopharmaceutical industry, there is a growing disconnect between the level of knowledge handled by a new...
It is recognized in the industry that unforeseen project costs can jeopardise a clinical trial’s continuity...
From planning to completion, clinical trial development deals with a large number of very narrow speciality fields.
Ophthalmology clinical research has seen a proliferation of exciting advances in recent years.
ISO 9001:2015 certification shows a company’s ability to consistently provide products
There is a high need to get more medications authorized for paediatric use.
Importing and exporting supplies for a clinical trial in Russia poses unique challenges. Learn how to handle them here.
Clinical trials are one of the most critical steps in the entire drug development process. Apart from a strong...
The process of marketing authorization is a crucial step in the entire drug development process. Deciphering the most...
Companies operating in regulated environments deliver a multitude of tasks while complying with regulatory mandates...
Industry leaders understand that keeping sufficient enrollment speed in clinical trials amidst the COVID-19...
The COVID-19 pandemic has caused widespread disruptions in the healthcare sector. While many industries faced...
The European Union is composed of 27 different countries who have agreed to keep close economic ties...
A Request for Proposal, or RFP, is a document soliciting bids from different contractors or service providers. Often...
When planning for a new clinical trial, the initial budget may be the first item that potential investors will look...
Dokumeds is a CRO highly experienced in TB clinical research and during 25 years in business, the company...
Learn how your clinical trials can take advantage of Europe’s healthcare infrastructure.
Patient recruitment is one of the trickiest and most time-sensitive aspects when conducting a clinical trial. Problems..
Pharmacovigilance has always been an integral part of drug development. The origins of pharmacovigilance go as far ...
Find out how we cut costs by streamlining enrollment
For many years, clinical research operations in South Africa have been quietly accelerating. Back in 2013, South Africa
Tuberculosis (TB) is a major global disease that is caused by a bacterium called Mycobacterium tuberculosis (MTB). TB ..
South Africa has a well-established research infrastructure and our new office will strengthen our global presence...
The Study Start-Up Group (SSUG) in Dokumeds Russia started operations in September 2015, and amazingly, has reduced ...
The European Union (EU) Medical Device Regulation (MDR) 2017/745 came into force in May 2021. The EU MDR currently...
The COVID-19 pandemic has had unprecedented implications on clinical trials and research, ranging from...
Rare diseases affect an estimated 3-6% of the global population, which may in fact be an underestimate...
Russia, due to its vast population, availability of qualified investigators, and advanced diagnostic and treatment...
According to the European Medicines Administration (EMA), approximately 50% of all medications routinely used...
From a management perspective, clinical trials are complex operations: they involve multiple stakeholders...
The European Union (EU) provides important geographical coverage in clinical research...
The high biological variability involved in cancer and the stringent regulatory requirements make clinical trials...
Clinical trials is a multinational industry, where teams from different backgrounds come together to collaborate...
The complexity of running a clinical trial requires the involvement of various experts to ensure its success...
Once the planning and start-up procedures for a clinical trial are completed, the most critical part of the trial...
In today’s biopharmaceutical industry, there is a growing disconnect between the level of knowledge handled by a new...
It is recognized in the industry that unforeseen project costs can jeopardise a clinical trial’s continuity...
From planning to completion, clinical trial development deals with a large number of very narrow speciality fields.
Ophthalmology clinical research has seen a proliferation of exciting advances in recent years.
Clinical trials are one of the most critical steps in the entire drug development process. Apart from a strong...
The process of marketing authorization is a crucial step in the entire drug development process. Deciphering the most...
Companies operating in regulated environments deliver a multitude of tasks while complying with regulatory mandates...
Industry leaders understand that keeping sufficient enrollment speed in clinical trials amidst the COVID-19...
The COVID-19 pandemic has caused widespread disruptions in the healthcare sector. While many industries faced...
The European Union is composed of 27 different countries who have agreed to keep close economic ties...
A Request for Proposal, or RFP, is a document soliciting bids from different contractors or service providers. Often...
When planning for a new clinical trial, the initial budget may be the first item that potential investors will look...
Dokumeds is a CRO highly experienced in TB clinical research and during 25 years in business, the company...
Patient recruitment is one of the trickiest and most time-sensitive aspects when conducting a clinical trial. Problems..
Pharmacovigilance has always been an integral part of drug development. The origins of pharmacovigilance go as far ...
For many years, clinical research operations in South Africa have been quietly accelerating. Back in 2013, South Africa
Tuberculosis (TB) is a major global disease that is caused by a bacterium called Mycobacterium tuberculosis (MTB). TB ..
The Study Start-Up Group (SSUG) in Dokumeds Russia started operations in September 2015, and amazingly, has reduced ...
Learn how to efficiently conduct your clinical study in Europe with our expert guide.
This e-book will provide you with key tips to successfully navigate pharmacovigilance for clinical trials in the EU
There is a high need to get more medications authorized for paediatric use.