Oct
2026
Fiera Milano, Italy
Visit us
stand 4A39, API

Suanfarma

Exhibitor at CPHI Milan 2026
About Us

Suanfarma founded in 1993, is a B2B life science partner committed to health & innovation by developing, manufacturing, and distributing high quality ingredients for the pharmaceutical industry, with 12 global offices serving over 400 clients in more than 70 countries.

At Suanfarma we provide comprehensive CDMO services for fermentation and chemical synthesis projects, offering a one-stop-shop solution with a proven track record for successful development, scaling, manufacturing, and commercialization of both innovative and generic APIs.

  • Country/Region:
    Spain
  • On CPHI since:
    2015
  • Certificates:
    3
  • Employees:
    250 - 499
Company types
CMO/CDMO
Distributor/Import Export
Manufacturer/Innovator
Primary activities
API Producer
Contract Manufacturer
Contact info
Event information
CPHI Milan 2026
  • 6 Oct 2026 - 8 Oct 2026
  • Fiera Milano, Italy
  • Visit us at stand 4A39, API

Products Featured at CPHI Milan 2026

  • LYMECYCLINE

    Product LYMECYCLINE

    Lymecycline is a second-generation oral tetracycline prodrug known for its broad-spectrum activity against both Gram-positive and Gram-negative bacteria. It is widely used in the treatment of acne and other susceptible bacterial infections, particularly where good tolerability is essential.

Suanfarma Resources (1)

  • Video Revolutionizing Pharma Manufacturing With TT&GO® Technology Transfer

    In the rapidly evolving landscape of pharmaceutical manufacturing, the TT&GO® platform by Suanfarma CDMO stands out as a revolutionary solution for technology transfer. This session will explore into the unique methodology of TT&GO®, which integrates rigorous, systematic procedures grounded in risk-based analysis to facilitate seamless technology transfers. Methodological rigor and flexibility: Understanding the systematic approach of TT&GO® that applies to various phases of the product lifecycle, ensuring adaptability and compliance with Good Manufacturing Practices (GMP). Risk management and cost efficiency: Analyzing how TT&GO®'s proactive risk assessment and mitigation strategies lead to reduced failure rates and cost savings, empowering clients to pursue ambitious project timelines with minimized risks. Real-world applications and outcomes: Presenting case studies and success stories of TT&GO® in action, highlighting the platform's impact on accelerating commercial launches and enhancing market competitiveness. Attendees of this session can expect to leave with a comprehensive understanding of how advanced technology transfer methodologies like TT&GO® can be leveraged to optimize pharmaceutical manufacturing processes, ensuring higher efficiency, reduced risk, and better overall outcomes.