We have compiled a list of manufacturers, distributors, product information, reference prices, and rankings for drug substance.
ipros is IPROS GMS ・ IPROS One of the largest technical database sites in Japan that collects information on.

drug substance Product List and Ranking from 10 Manufacturers, Suppliers and Companies

Last Updated： Aggregation Period:Nov 05, 2025～Dec 02, 2025
This ranking is based on the number of page views on our site.

drug substance Manufacturer, Suppliers and Company Rankings

Last Updated： Aggregation Period:Nov 05, 2025～Dec 02, 2025
This ranking is based on the number of page views on our site.

  1. null/null
  2. 大塚化学 Tokyo//Chemical
  3. 立山化成 Toyama//Manufacturing and processing contract
  4. 4 Cytiva Tokyo//others
  5. 4 桂化学 Kanagawa//others
Go to Company Ranking

drug substance Product ranking

Last Updated： Aggregation Period:Nov 05, 2025～Dec 02, 2025
This ranking is based on the number of page views on our site.

  1. Pharmaceutical CDMO services 大塚化学
  2. Development of various types of medium-sized molecule (nucleic acid, peptide) pharmaceuticals (processes, analytical methods, etc.)
  3. Freeze & Go Solutions Cytiva
  4. 4 Ouchi Shinko Chemical Industry Co., Ltd. 須賀川市 経済環境部商工課
  5. 4 Contract development and manufacturing (CDMO) business for mid-sized molecules (oligonucleotides and peptides) active pharmaceutical ingredients.

drug substance Product List

16～18 item / All 18 items

Displayed results
Fundamentals and Applications of Process Chemistry (Organic Synthesis) in Pharmaceutical Development

Fundamentals and Applications of Process Chemistry (Organic Synthesis) in Pharmaceutical Development

What should be considered to understand process chemistry and establish an effective manufacturing method compliant with GMP? Efforts in the lab? Scale-down.

Lecturer Representative Director of Pharmaceutical Research and Development Consulting, Mr. Mitsuki Hashimoto Target Audience: Individuals responsible for process chemistry in pharmaceutical development facing challenges Venue: Kawasaki City Educational and Cultural Center, Room 3 [Kanagawa, Kawasaki] 12 minutes on foot from JR Kawasaki Station, 10 minutes on foot from Keikyu Kawasaki Station Date and Time: April 27, 2011 (Wednesday) 10:30 AM - 4:00 PM [Individual Consultation: 4:00 PM - 4:30 PM (Reservation required)] Capacity: 30 people *Registration will close once full. Please apply early.

  • Company：AndTech
  • Price：10,000 yen-100,000 yen
  • Technical Seminar

Added to bookmarks

Bookmarks list

Bookmark has been removed

Bookmarks list

You can't add any more bookmarks

By registering as a member, you can increase the number of bookmarks you can save and organize them with labels.

Free membership registration
Tateyama Chemical Co., Ltd. Quality Assurance System

Tateyama Chemical Co., Ltd. Quality Assurance System

With "creative practice" as a keyword, we are constantly reevaluating our quality assurance system.

Our company started with the production of methyl ephedrine, an active pharmaceutical ingredient (API) for expectorants. The manufacturing of APIs and their quality control are the very roots of Tateyama Chemical. Aiming for world-class quality assurance, we achieve global-level quality assurance that complies not only with Japan's GMP, which is the standard for pharmaceutical manufacturing and quality control, but also with PIC/S GMP, to supply safe, effective, and high-quality pharmaceuticals to countries around the world. To respond to the trust of various customers and ultimately the end users, we will continuously update our quality control system. 【Management Policy】 ■ Development of new products ■ Refinement of technology ■ Thorough implementation of 5S and quality control ■ Raising awareness of environmental conservation and health and safety *For more details, please refer to the PDF materials or feel free to contact us.

  • Contract manufacturing
  • Chemicals

Added to bookmarks

Bookmarks list

Bookmark has been removed

Bookmarks list

You can't add any more bookmarks

By registering as a member, you can increase the number of bookmarks you can save and organize them with labels.

Free membership registration
[CPhI Seminar Report] Mutagenic Impurities in Pharmaceuticals (Active Pharmaceutical Ingredients)

[CPhI Seminar Report] Mutagenic Impurities in Pharmaceuticals (Active Pharmaceutical Ingredients)

Development of testing methods and analysis examples! Established over 300 analytical methods that can guarantee PMI residues below 10 ppm!

At "CPhI Japan 2022," we held a presentation in our booth regarding ICH M7 compliance from the Development and Analytical Research Headquarters. We introduced the day's content, including "About ICH M7," "For the Development of Trace Analysis Methods," and "Examples of Method Validation." Please take a moment to read it. [Contents] ■ About ICH M7 ■ For the Development of Trace Analysis Methods ■ Examples of Method Validation ■ Conclusion *For more details, please refer to the related links page or feel free to contact us.

  • Other Testing Contract

Added to bookmarks

Bookmarks list

Bookmark has been removed

Bookmarks list

You can't add any more bookmarks

By registering as a member, you can increase the number of bookmarks you can save and organize them with labels.

Free membership registration

Related Categories of drug substance

COPYRIGHT © 2001-2025 IPROS CORPORATION ALL RIGHTS RESERVED.