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Contenido proporcionado por Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal. Todo el contenido del podcast, incluidos episodios, gráficos y descripciones de podcast, lo carga y proporciona directamente Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal o su socio de plataforma de podcast. Si cree que alguien está utilizando su trabajo protegido por derechos de autor sin su permiso, puede seguir el proceso descrito aquí https://es.player.fm/legal.
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Ravi Samavedam: On demand clean rooms for clinical trial supply

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Manage episode 382347589 series 3526489
Contenido proporcionado por Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal. Todo el contenido del podcast, incluidos episodios, gráficos y descripciones de podcast, lo carga y proporciona directamente Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal o su socio de plataforma de podcast. Si cree que alguien está utilizando su trabajo protegido por derechos de autor sin su permiso, puede seguir el proceso descrito aquí https://es.player.fm/legal.

This week we speak to Ravi Samavedam, Chief Innovation Officer for Azzur Group, about how on demand clean rooms can transform the business model for biotechs.

We start out by exploring what the standard two choices biotech’s typically have for clinical trial manufacturing:

  1. Building their own infrastructure
  2. Outsourcing to a contract manufacturing organization

Both options have pros and cons. Many of the cons can be mitigated by the third option that Ravi suggests - renting the infrastructure. This enables the biotech to keep control with the manufacturing process and keep experimenting, while avoiding the upfront investment in the infrastructure that may change.

We also dive into the compliance of the facilities, and how outsourcing the quality assurance of the facilities themselves can allow the biotech’s to focus on the production process and science.

Even though the clean rooms for the different companies are in the same facilities, there is no exchange of air or supplies between the rooms - and also limited exchange of ideas between the individual production lines due to confidentiality.

As a small biotech it is easy to fall into the trap of going overboard with GMP regulation adherence. And how GMP stamina is necessary to know where to draw the line of sufficient quality.

Guest:

Ravi Samavedam

https://www.linkedin.com/in/ravi-samavedam-65a8345/

Azzur

https://azzur.com/

________
Reach out to Sam Parnell and Ivanna Rosendal
Join the conversation on our LinkedIn page

  continue reading

66 episodios

Artwork
iconCompartir
 
Manage episode 382347589 series 3526489
Contenido proporcionado por Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal. Todo el contenido del podcast, incluidos episodios, gráficos y descripciones de podcast, lo carga y proporciona directamente Sam Parnell & Ivanna Rosendal, Sam Parnell, and Ivanna Rosendal o su socio de plataforma de podcast. Si cree que alguien está utilizando su trabajo protegido por derechos de autor sin su permiso, puede seguir el proceso descrito aquí https://es.player.fm/legal.

This week we speak to Ravi Samavedam, Chief Innovation Officer for Azzur Group, about how on demand clean rooms can transform the business model for biotechs.

We start out by exploring what the standard two choices biotech’s typically have for clinical trial manufacturing:

  1. Building their own infrastructure
  2. Outsourcing to a contract manufacturing organization

Both options have pros and cons. Many of the cons can be mitigated by the third option that Ravi suggests - renting the infrastructure. This enables the biotech to keep control with the manufacturing process and keep experimenting, while avoiding the upfront investment in the infrastructure that may change.

We also dive into the compliance of the facilities, and how outsourcing the quality assurance of the facilities themselves can allow the biotech’s to focus on the production process and science.

Even though the clean rooms for the different companies are in the same facilities, there is no exchange of air or supplies between the rooms - and also limited exchange of ideas between the individual production lines due to confidentiality.

As a small biotech it is easy to fall into the trap of going overboard with GMP regulation adherence. And how GMP stamina is necessary to know where to draw the line of sufficient quality.

Guest:

Ravi Samavedam

https://www.linkedin.com/in/ravi-samavedam-65a8345/

Azzur

https://azzur.com/

________
Reach out to Sam Parnell and Ivanna Rosendal
Join the conversation on our LinkedIn page

  continue reading

66 episodios

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