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Category: Other Blogs

Emergency Use Authorization Consulting

Why should you choose Emergency Use Authorization (EUA) consulting?

By Kim Fayett

  08/09/2020

  Category: Other Blogs

Many companies are utilizing emergency use authorization, or EUA, to get medical products to FDA for the U.S. marketplace. It is a...

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pharma consulting

What is biotech consulting and how does it benefit the pharma industry?

By KIm Fayett

  07/16/2020

  Category: Other Blogs

Biotechnology and pharmaceuticals are both technologies used in develop medical treatments. Often a biotechnology company uses living organisms/cells for the development of...

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FDA labels

How to develop FDA labeling for regulated products?

By Kelly Shelton

  07/06/2020

  Category: Other Blogs

U.S. food and drug labeling are to be compliant with the rules and guidelines of the Food and Drug Administration (FDA). FDA...

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Pharma Consulting Service

How to Choose a Pharmaceutical Consulting Service?

By Kelly Shelton

  06/15/2020

  Category: Other Blogs

Day-by-day new insights into diseases are made. New drugs, devices, biologics and new uses for old products are introduced to the marketplace...

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FDA fast track

An Overview of FDA Fast Track

By Kelly Shelton

  06/09/2020

  Category: Other Blogs

FDA consultants, like Biotech Research Group, can provide support and regulatory submissions for FDA fast track service. FDA Fast Track is a...

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Hand Sanitizer consulting

Search trend in 2020: Basic prevention from COVID-19?

By Kelly Shelton

  06/04/2020

  Category: Other Blogs

SARS-CoV-2 leading to the coronavirus-associated disease, COVID-19, is highly contagious. The aerosolized transmission explains the speed with which it has spread around...

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Hand Sanitizer consulting

Coronavirus transmission: how to protect yourself from coronavirus?

By

  05/26/2020

  Category: Other Blogs

Coronaviruses are a family of viruses that can be pathogenic for humans and animals. In humans, several coronaviruses are known to cause...

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FDA pre-submission program

Device Details: FDA Pre-submission programs and in vitro diagnostics

By Kelly Shelton

  05/19/2020

  Category: Other Blogs

Medical devices are essential tools for human medicine. They are intended, by their manufacturer, to be used with medical advice/administration and provide...

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Drug Post Launch Activity

Post Launch Activity – How is a new drug developed and tested, even after approval? Know the end-to-end process

By Kelly Shelton

  05/12/2020

  Category: Other Blogs

This is a question that many of us, as patients or family members of people with rare diseases in particular, ask ourselves....

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medical device expert

510(k): How to evaluate the needs for medical device compliance?

By Kelly Shelton

  05/07/2020

  Category: Other Blogs

The techniques and methods used in device evaluations depend on the type of specific product. Devices are diverse in nature in components...

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Global Experts in biotechresearchgroup

IND consulting and regulations

By Kelly Shelton

  05/02/2020

  Category: Other Blogs

During the development of a new drug, a sponsor should determine whether the product is safe for early use in humans and...

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Quality Assurance & Quality Control

Stay active in biopharmaceutical innovation, development, production and quality assurance

By Kelly Shelton

  04/22/2020

  Category: Other Blogs

Creating and producing biopharmaceuticals is expensive and difficult. As products move into the global maze of differing and sometimes changing government regulations,...

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