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Category: Other Blogs

pharmaceutical consulting firms

What are Regulatory Affairs Services and How to Maintain Regulatory Compliance?

By Kelly Shelton

  04/14/2020

  Category: Other Blogs

Regulatory affairs services are used to comply with protecting public health, and they can contribute to the safety and efficacy of medical-related...

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Medical device consulting

Medical device consultants and quality assurance advice

By Kelly Shelton

  04/10/2020

  Category: Other Blogs

Quality assurance services include identifying quality metrics, ensuring continuous improvements, and aligning with your business needs and objectives. Medical device subsystem consultants...

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FDA Approvals

FDA Drug labeling and prescription medications – FDA Approvals

By Kelly Shelton

  04/02/2020

  Category: Other Blogs

Since 2006, there has been a labeling redesign from the past FDA drug labeling program. Drug labeling is now presented as a...

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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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