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Staying Compliant in a Changing World: Best Practices with Niyati Patel

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Manage episode 382905138 series 3446111
Content provided by Harsh Thakkar. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Harsh Thakkar or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Episode 027: Harsh Thakkar (@harshvthakkar) interviews Niyati Patel (@niyatipatel), the Director of Quality Engineering at Getinge (Maquet Cardiovascular) and a Sr. Regulatory/ Quality Consultant at Compliance Insight, Inc.
Niyati breaks down the complexities of quality management systems, compliance, and regulations in the industry. She discusses the unique challenges companies face, especially when dealing with drugs, devices, and combination products, and emphasizes the importance of expert consultation and the use of technology in achieving compliance.
Harsh and Niyati debate the differences between a QMS and a BMS and the strengths of each. They elaborate on how a robust QMS acts as the backbone of a company's compliance strategy, integrating various processes and ensuring they are up to par with regulatory standards.
-----
Links:
*Compliance Insight, Inc.
*Compliance Insight, Inc. LinkedIn
*Getinge
*Would you rather watch the video episode? Subscribe to full-length videos on our YouTube channel.
-----
Show Notes:
(6:56) Integrating BMS and QMS in various industries.
(11:31) Regulations for combination products and their unique challenges.
(19:24) Drug and device regulations for small startups.
(24:56) Software selection for biotech companies.

For more, check out the podcast website - www.lifesciencespod.com

  continue reading

Chapters

1. Staying Compliant in a Changing World: Best Practices with Niyati Patel (00:00:00)

2. Integrating BMS and QMS in various industries. (00:06:56)

3. Regulations for combination products and their unique challenges. (00:11:31)

4. Drug and device regulations for small startups. (00:19:24)

5. Software selection for biotech companies. (00:24:56)

52 episodes

Artwork
iconShare
 
Manage episode 382905138 series 3446111
Content provided by Harsh Thakkar. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Harsh Thakkar or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.

Episode 027: Harsh Thakkar (@harshvthakkar) interviews Niyati Patel (@niyatipatel), the Director of Quality Engineering at Getinge (Maquet Cardiovascular) and a Sr. Regulatory/ Quality Consultant at Compliance Insight, Inc.
Niyati breaks down the complexities of quality management systems, compliance, and regulations in the industry. She discusses the unique challenges companies face, especially when dealing with drugs, devices, and combination products, and emphasizes the importance of expert consultation and the use of technology in achieving compliance.
Harsh and Niyati debate the differences between a QMS and a BMS and the strengths of each. They elaborate on how a robust QMS acts as the backbone of a company's compliance strategy, integrating various processes and ensuring they are up to par with regulatory standards.
-----
Links:
*Compliance Insight, Inc.
*Compliance Insight, Inc. LinkedIn
*Getinge
*Would you rather watch the video episode? Subscribe to full-length videos on our YouTube channel.
-----
Show Notes:
(6:56) Integrating BMS and QMS in various industries.
(11:31) Regulations for combination products and their unique challenges.
(19:24) Drug and device regulations for small startups.
(24:56) Software selection for biotech companies.

For more, check out the podcast website - www.lifesciencespod.com

  continue reading

Chapters

1. Staying Compliant in a Changing World: Best Practices with Niyati Patel (00:00:00)

2. Integrating BMS and QMS in various industries. (00:06:56)

3. Regulations for combination products and their unique challenges. (00:11:31)

4. Drug and device regulations for small startups. (00:19:24)

5. Software selection for biotech companies. (00:24:56)

52 episodes

All episodes

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