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Healthcare e-Commerce Market Size, Overview, Share and Forecast 2031

Posted by Prajakta on April 23, 2024 at 7:44am 0 Comments

The Healthcare e-Commerce Market in 2023 is US$ 253.88 billion, and is expected to reach US$ 1109.94 billion by 2031 at a CAGR of 20.25%.

FutureWise Research published a report that analyzes Healthcare e-Commerce Market trends to predict the market's growth. The report begins with a description of the business environment and explains the commercial summary of the chain… Continue
Veena Dimak
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Veena Dimak posted a blog post

Why India is among the first choices for Clinical Trials? | Clinical Research Courses

In the context of world, current hectic lifestyle of people has led to an increase in variety of diseases and illnesses. Recent pandemic experience taught everyone how having a strong immunity would help in effective treatment of even one of the most transmittable viruses. This scenario could not be applied to other serious illnesses that require proper medical attention. (Clinical Research Courses)What is…See More
Sep 3, 2022
Veena Dimak posted a blog post

Adopt These Functions to fix Clinical Trial Delays

Implementing a clinical trial involves rigorous research and extensive resource employment. In the process, trials may take up more time than anticipated, which adds to the running costs. Thus, specific functions are put in place to improve the profitability of clinical research by adopting a wider perspective. A few common factors that trigger delays in clinical trials are:• Differences in management of procedures: The burden of responsibility over the shoulders of clinical trials is increased…See More
Aug 22, 2022
Veena Dimak posted a blog post

5 Stepped-Protocol for the Drug Development | Clinical Research Courses

The drug development process still remains one of the prominent areas that requires intensive research for creating effective pharmaceutical products. This pharmaceutical industry needs to be constantly upgraded with time to help human bodies adapt for novel diseases. Here are 5 steps that are followed to create the medicine or drugs following a set of protocols:Step I: Discovery & developmentNew…See More
Aug 12, 2022
Veena Dimak posted a blog post

5 Reasons to get enrolled in Clinical Data Management Course by TechnoBridge

Overview:With the recent Covid-19 pandemic experience, it has become a need of the hour to emphasize on clinical research. Many governments of several countries have spent huge amounts of money into the clinical trials to gather information on developing medications and vaccines. This is where the role of Clinical Data Management (CDM) comes into the picture. The main role of CDM teams is to provide relevant…See More
Jul 21, 2022
Veena Dimak posted a blog post

How Clinical Research Courses are shaping upcoming professionals in the clinical field

Introduction In simpler words, clinical research is a type of investigation that covers all areas of treatment, diagnosis, prevention and curing diseases. It could also be said that majority of practicing doctors and professionals would be familiar more with the results of a clinical trial than medical journals. In order to start your journey as a clinical research professional, get to know more about Clinical…See More
Jul 19, 2022
Veena Dimak posted a blog post

Clinical Research Scope& Career Opportunities in the Industry

What is Clinical Research?Clinical research is a process of testing the safety and efficacy of drugs and other medical products. It is done by qualified professionals who are responsible for the design, conduct, analysis, and reporting of clinical trials.Clinical research is a process that ensures the safety and efficacy of drugs and other medical products. Clinical research professionals are responsible for designing, conducting, analyzing, and reporting clinical trials that test these…See More
May 11, 2022
Veena Dimak posted a blog post

Scope, Role of Regulatory Affairs & How to get Job in Regulatory Affair Industry

Overview of Regulatory AffairsDrug regulatory affairs is the process of ensuring that a product or medicine is safe for public use.The drug regulatory affairs department is responsible for ensuring that all aspects of the drug's development and production meet with local, regional, national, and international regulations. They also monitor any changes in the manufacturing process to ensure that they are…See More
Apr 13, 2022
Veena Dimak posted a blog post

What Are the Different Types of Clinical Research?

Treatment ResearchTreatment research is a branch of medical research that focuses on the discovery, development and evaluation of treatments for diseases.In the field of treatment research, there are a wide range of methods that are used in order to find new treatments for diseases. These methods include clinical trials, animal models, and bench-to-bedside translational and basic science research.The goal of…See More
Apr 11, 2022
Veena Dimak posted blog posts
Apr 7, 2022
Veena Dimak posted blog posts
Apr 5, 2022
Veena Dimak posted a blog post

A New Era of Pharmacovigilance Future Opportunities and Challenges

Introduction to PharmacovigilancePharmacovigilance is an important part of the drug development process, and it ensures that the benefits of the drugs outweigh the risks. It includes monitoring a drug's safety after it has been approved for marketing, and identifying any adverse effects that may not have been known before. Pharmacovigilance is one of the most important parts of drug development. It ensures…See More
Apr 1, 2022
Veena Dimak posted blog posts
Mar 31, 2022
Veena Dimak posted a blog post

What is Pharmacovigilance? Why Pharmacovigilance Courses is important?

What is Pharmacovigilance? Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems. It also includes the entire process of collecting data on a medicine's safety profile. Pharmacovigilance is a science that deals with the detection, assessment, understanding and prevention of adverse effects or…See More
Mar 24, 2022
Veena Dimak posted a blog post

Scope | Overview | How to Become Clinical Research Professional?

Overview of Clinical Research Clinical research is the process of investigating the safety and effectiveness of new drugs, devices, and other treatments. A clinical trial is a research study that tests new treatments or therapies that are intended to prevent, diagnose, or treat various conditions. It can also be used to test a new drug for safety and efficacy. Clinical trials are usually overseen by one or…See More
Mar 23, 2022
Veena Dimak posted a blog post

Regulatory Affairs in Covid-19 | Uses | Circes

What is Regulatory Affairs?Regulatory affairs is a term used to describe the process of ensuring that a drug or medical device is safe and effective for use by humans. The regulatory affairs function includes many different roles and responsibilities, including clinical research, product approval, labelling/marketing/promotion, quality assurance, and post-market surveillance. Regulatory Affairs…See More
Mar 21, 2022
Veena Dimak posted blog posts
Mar 7, 2022

Veena Dimak's Blog

Why India is among the first choices for Clinical Trials? | Clinical Research Courses

Posted on September 3, 2022 at 4:19am 0 Comments

In the context of world, current hectic lifestyle of people has led to an increase in variety of diseases and illnesses. Recent pandemic experience taught everyone how having a strong immunity would help in effective treatment of even one of the most transmittable viruses. This scenario could not be applied to other serious illnesses that require proper medical attention. (Clinical Research… Continue

Adopt These Functions to fix Clinical Trial Delays

Posted on August 22, 2022 at 6:41am 0 Comments

Implementing a clinical trial involves rigorous research and extensive resource employment. In the process, trials may take up more time than anticipated, which adds to the running costs. Thus, specific functions are put in place to improve the profitability of clinical research by adopting a wider perspective. A few common factors that trigger delays in clinical trials are:

• Differences in management of procedures: The burden of responsibility over the shoulders of clinical trials is… Continue

5 Stepped-Protocol for the Drug Development | Clinical Research Courses

Posted on August 12, 2022 at 6:26am 0 Comments

The drug development process still remains one of the prominent areas that requires intensive research for creating effective pharmaceutical products. This pharmaceutical industry needs to be constantly upgraded with time to help human bodies adapt for novel diseases. Here are 5 steps that are followed to create the medicine or drugs following a set of protocols:

Step I: Discovery &… Continue

5 Reasons to get enrolled in Clinical Data Management Course by TechnoBridge

Posted on July 21, 2022 at 4:03am 0 Comments

Overview:

With the recent Covid-19 pandemic experience, it has become a need of the hour to emphasize on clinical research. Many governments of several countries have spent huge amounts of money into the clinical trials to gather information on developing medications and vaccines. This is where the role of Clinical Data Management (CDM) comes into the picture. The main role of CDM teams is to provide… Continue

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