February 4, 2021
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
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
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
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
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
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
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
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
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
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. […]
April 25, 2020
Clinical trials take up the last half of the 10 – 15 year, 1.5 – 2.0 billion USD, cycle of development just for introducing […]
May 12, 2020
Notice to Applicants The European Commission in tandem with proficient authorities from the Member States, the European Medicines Agency along with interested parties created the Notice […]
May 12, 2020
In Brief The necessity of the risk management plan (RMP) has been studied before the launch of the medical device and medicinal product. Risk management documents/plan […]
June 20, 2020
In brief: The major steps in conducting a clinical trial study are study design, study conduct, data analysis and reporting of the findings. Randomized clinical trials […]
June 24, 2020
What is Product cycle? In pharmaceutical industry, product cycle consists of all processes from drug discovery to launch to access, which is closely monitored by […]
June 30, 2020
SaMD or Software as a Medical Device can be described as a software constructed to be used in medical devices. These softwares can be run […]
July 6, 2020
In brief: The clinical study protocol is defined as the procedures by which clinical research is conducted A clinical study protocol should provide a clear […]
July 17, 2020
In brief Health data contains important information that can help save lives and cro biostatistics services provide information to support public health initiatives. Biostatisticians […]
July 25, 2020
In brief Clinical research studies the effect of an intervention on a specific population or the causation-association between a predicting variable and a health condition. The […]
December 18, 2020
In-Brief: Does the need for protection of patients and public health increasing? Unquestionably yes. The science of regulating and understanding this process is known as pharmacovigilance […]