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Category: Other Blogs

FDA 510k System And 510 K Premarket Notification Devices

The FDA 510(k) Premarket Notification for Devices

By Kelly Shelton

  02/26/2020

  Category: Other Blogs

In general, the 510 k premarket notification for devices in the U.S. marketplace are clearances by FDA as findings of substantial equivalence...

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Professional Pharma Consulting And Pharmaceutical Research Services

Professional Pharmaceutical Consulting and Research Services

By Kelly Shelton

  02/20/2020

  Category: Other Blogs

Companies should choose pharmaceutical consulting that allows for special attention to unique differences to position a product at the lowest cost to...

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medical device subsystem consultants

Strategies to Meet the Expectations of FDA Device Policies

By Kelly Shelton

  02/06/2020

  Category: Other Blogs

With the advancement of technology, a wide variety of medical devices that have increasing complexity and diversity should also increase the benefits...

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FDA Validation

Principle of Quality Assurance of a Drug Set by FDA (FDA validation)

By Kelly Shelton

  01/28/2020

  Category: Other Blogs

Food and Drug Administration (FDA) is responsible for monitoring, analyzing, and testing pharmaceutical human and animal drug production and ensure that the...

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FDA Warning Letters

FDA Warning Letters – Initiative Taken by FDA for Violating the Quality Standards

By Kelly Shelton

  01/21/2020

  Category: Other Blogs

United States Food and Drug Administration send an official message to the particular manufacturer or the organization on account of violating any...

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FDA Establishment Registration

General Facts About FDA Establishment Registration

By Kelly Shelton

  01/08/2020

  Category: Other Blogs

The abbreviated form of FDA is food and drug administration. It is a US health information organization. The FDA is involved in...

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FDA Dietary Supplement

Duties of FDA Dietary Supplement Health And Education Act

By Kelly Shelton

  12/27/2019

  Category: Other Blogs

FDA was abbreviated as the food and drug administration. The duty FDA is to evaluate and approves many different things such as...

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FDA Adverse Event Reporting

What are The Main Purposes of FDA Adverse Event Reporting?

By Kelly Shelton

  12/21/2019

  Category: Other Blogs

The US FDA (Food and drug administration) is in charge of upholding patients and defending public health by guarantee the safety, security...

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Clinical Research Consultant

Various Duties of Clinical Research Consultant

By Kelly Shelton

  12/14/2019

  Category: Other Blogs

The medical research organization will provide a comprehensive and quality consulting service. This consultant service is essential for clinical research and statistical...

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FDA OTC drugs consulting services

Know the process through which an OTC drug undergoes before it is made available in the market

By Kelly Shelton

  11/05/2019

  Category: Other Blogs

The food, drug and Cosmetic Act (FDC) were started in the year 1938, and it also allowed that the medical products that...

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Tips to follow for successful 510(k) submission

Tips to follow for successful 510k submission

By Kelly Shelton

  10/21/2019

  Category: Other Blogs

For companies who are not prepared to submit a 510k regulatory clearance, then the procedure can be painful for you. We have...

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regulatory affairs services

Thinking of becoming a Regulatory Affairs Officer? Know the Key Points

By Kelly Shelton

  10/15/2019

  Category: Other Blogs

Did you know? You cross with the regulatory affairs industry almost daily, but don’t observe it. Each food product, beverage, or a...

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