Electronic Trial Master File

Electronic Trial Master File

Methods of Capturing the data  clinical trials.

Electronic Trial Master File (eTMF) solution is a clinical collaboration platform for managing the Data of Subject, Activity, Tracking, Maintaining, Archiving clinical trial documents. It allows life sciences companies to streamline processes, automate information exchange, and reduce the administrative overhead associated with running clinical trials.

What EDC Gives:

  • eTMF Process Management and Workflow of the Activity Wise Management
  • In an eTMF,

Electronic Data Capture in Biznet

Methods of Capturing the data  clinical trials.

When researchers conduct a clinical study, they collect information about their patients using Case Report Forms (CRFs).

After the conduction of clinical Trials or BA/BE studies the large numbers of forms like CRF, Protocol, ICD, Insurance Policy, Source documents, Master documents were required for the study as well as the Audit purpose for the regulatory.

Biolyte for Bioanalytical Solution

Biolyte for Bioanalytical Solution

Introduction:
The development of the bioanalytical techniques brought a progressive discipline for which the future holds many exciting opportunities to further improvement. The main impact of bioanalysis in the pharmaceutical industry is to obtain a quantitative measure of the drug and its metabolites. The purpose is to perform the pharmacokinetics, toxicokinetic, bioequivalence and exposure response like Various bioanalytical technique performed in bioanalytical studies such as hyphenated techniques,

Why Smart R (IWRS) in Clinical Research?

Clinical research and the pharmaceutical industry have been exponentially expanded throughout the first decade of the 21st century in terms of drug revelations, their inventions, several medical devices, and other technologies to assist the community better in health care. 

This accelerated boom has put pharmaceutical industries under enormous pressure to win the race by getting their drugs in the market and getting them patented.

clinical trials for efficient patient care

Software use for efficient patient care in clinical trials

A new test product and treatment both aren’t sold in the market directly. Before the sell, it needs to be tested on research subjects for efficacy, safety, tolerability of different dosage forms and diseases studied for this whole process is called a Clinical Trial.

In the whole process of conducting clinical trials there are some necessary approvals required from the applicable regulatory,

Clinical Data using technology as a solution in setting benchmark

Clinical Data using technology as a solution in setting benchmark

It has become a practice now to avoid data slip through cracks, where CROs have been continuously evolving by moving towards technology as a solution for their data capturing from scratch to the end report. Recent findings in tech world has highlighted the power of machine learning algorithms and their impact on Clinical Trials company assaying bigger capabilities to ensure data integrity and quality.

Regulatory compliant, multi-functional Clinical trials management software solution for CROs

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