Greeting
PPG was founded start as a consulting company focusing on the Life Sciences regulatory area. Mr. Takeshi Adachi, founder and CEO, has many years of experience in the pharmaceutical industry.
Services provided include general consulting with a special focus on small startup companies in the spirit of “projetista”.
PPG main services are:
- Regulatory support of Pharmaceutical/Medical device and re-generative medicine products development (PMDA Consultation Meeting, CTN, NDA submission, PMDA review process）
- IT implementation project support (e.g. eCTD）
PPG will provide consulting services on flexible terms – from short term on demand hourly engagements to long term retainer-based contracts.
Please contact us to inquire about our flexible services. PPG would like to support your company to achieve you’re a brilliant future.
PPG Inc.
CEO Takeshi Adachi
CEO Introduction
Takeshi Adachi is CEO and founder of PPG.
Takeshi has over 20 years of experience in the pharmaceutical industry. He has held senior level positions in several pharmaceutical companies in departments including regulatory, pharmacovigilance and PMS (post marketing surveillance).
He started his career as an analytical scientist and developed several analytical methods for new chemical entities including LC/MS. After this experience, he moved to the regulatory area of new drug development. He has many years of product development and NDA experience for new pharmaceutical drug products. In addition, he has extensive risk and crisis management experience including product recalls, DHCP letters, and regulatory reports of pharmaceutical AE and medical devices defects.
He was the ICH M2 JPMA Topic Leader and he lead the implementation of eCTD in the Japan pharmaceutical industry. He is experienced in implementation projects for eCTD production and Document management systems.
Takeshi studied Pharmacy at the University of Kanazawa and he also studied the Business at University of Business Breakthrough. He is a pharmacist and holds a master’s degree in business administration.
Job Carrier
| 1987 – 1996 | Analytical scientist, Laboratory of Taisho Pharmaceutical Co., Ltd. |
| 1996 – 2001 | Regulatory liaison, Taisho Pharmaceutical Co., Ltd. |
| 2001 – 2004 | Group Manager, Regulatory Development Strategy, Aventis Pharma Co. Ltd. |
| 2004 – 2006 | Deputy Head of Pharmacovigilance and head of PMS, Sanofi-Aventis K.K. |
| 2006 – 2011 | Regulatory Director, Janssen pharmaceutical K.K. |
Registered pharmacist, MBA
Industry Activity and Responsibility
| 1998 -2003 | Join JPMA ESMI (electronic standard for medicinal information) group. Join eCTD Project. |
| 2003 – 2010 | Join JPMA ICH project. M2 expert and Topic leader |
| 2006 – 2010 | Leader of JPMA Electronic Information sub-committee |
| 2007 – 2010 | Member of discussion group for medicinal information network in MHLW |
| 2006 – 2010 | ISO215 member in Japan |
| 2010 – 2014 | Board Member of NPO Public ware promotion |