pepgra

February 4, 2021

What are the EMA Guidelines for Clinical Trial Management?

In Brief Clinical trials are the scientific way of assessing medications’ efficacy in treating a medical condition and side effects. EMA guidelines for clinical trial regulations […]

February 1, 2021

How to identify and recruit patients for secured clinical trials? Top 10 tips

In-Brief: The best clinical trial recruitment strategies start by focusing on the patient perspective. From there, it helps to get creative. A reliable clinical trial patient […]

January 28, 2021

Literature Review of Drug Development using Real-World Evidence

In-Brief: Real-world evidence, which is based on data gathered during routine clinical exercise, has the potential to make a significant impact in nearly every phase of […]

January 25, 2021

Reporting Side Effects for Any Medical Products, Devices or Drugs

Brief Humans differ in their biological reactions to medical products or drugs but not all adverse reactions associated with the use of medical products can be […]

January 22, 2021

How regulatory writing plays an essential role in clinical research?

In-Brief: There are two main parts in medical writing, medical communication and regulatory writing. Pepgra blog focuses on regulatory writing, which involves preparing the clinical study and […]

January 18, 2021

How Electronic Health Records transforms the Healthcare Sectors?

Brief: Advancements in the medical field and the proliferation of diagnosis and screening tests have to create mountains of data on patient healthcare. Digital information technology […]

January 18, 2021

Practical Guidance for Biomarkers into Early Phase Clinical Research Purposes

In-Brief: Healthcare data analytics solutions provide a powerful approach to understand the spectrum of disease with applications in observational and analytic epidemiology, screening and diagnosis randomized […]

January 11, 2021

Uses of Patient Registries for Clinical Studies to Acquire Unwavering Data

In-Brief: The patient registry is a specific study or a detailed survey of research question or hypothesis generally. Clinical research statistical service is a collection of […]

January 7, 2021

Post authorization studies for clinical research purposes

Brief: Have a look at post-authorization safety studies and important pharmacoepidemiological and pharmacovigilance aspects in clinical research in this Pepgra blog. PASS covers different types […]

January 4, 2021

Recent trends in genomic biomarkers

Brief: Cardiovascular disease is a significant health concern worldwide despite having many genomics developments providing valuable new candidates for better biomarkers and novel therapeutic targets. […]

February 4, 2021

What are the EMA Guidelines for Clinical Trial Management?

In Brief Clinical trials are the scientific way of assessing medications’ efficacy in treating a medical condition and side effects. EMA guidelines for clinical trial regulations […]

February 1, 2021

How to identify and recruit patients for secured clinical trials? Top 10 tips

In-Brief: The best clinical trial recruitment strategies start by focusing on the patient perspective. From there, it helps to get creative. A reliable clinical trial patient […]

January 28, 2021

Literature Review of Drug Development using Real-World Evidence

In-Brief: Real-world evidence, which is based on data gathered during routine clinical exercise, has the potential to make a significant impact in nearly every phase of […]

January 25, 2021

Reporting Side Effects for Any Medical Products, Devices or Drugs

Brief Humans differ in their biological reactions to medical products or drugs but not all adverse reactions associated with the use of medical products can be […]

January 22, 2021

How regulatory writing plays an essential role in clinical research?

In-Brief: There are two main parts in medical writing, medical communication and regulatory writing. Pepgra blog focuses on regulatory writing, which involves preparing the clinical study and […]

January 18, 2021

How Electronic Health Records transforms the Healthcare Sectors?

Brief: Advancements in the medical field and the proliferation of diagnosis and screening tests have to create mountains of data on patient healthcare. Digital information technology […]

January 18, 2021

Practical Guidance for Biomarkers into Early Phase Clinical Research Purposes

January 11, 2021

Uses of Patient Registries for Clinical Studies to Acquire Unwavering Data

In-Brief: The patient registry is a specific study or a detailed survey of research question or hypothesis generally. Clinical research statistical service is a collection of […]

January 7, 2021

Post authorization studies for clinical research purposes

Brief: Have a look at post-authorization safety studies and important pharmacoepidemiological and pharmacovigilance aspects in clinical research in this Pepgra blog. PASS covers different types […]

January 4, 2021