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Main Camp

Zhejiang Hengdian Apeloa operates 7 API manufacturing facilities in China, serving global pharmaceutical markets with R&D, contract manufacturing and regulatory compliance.

Presentation of Main Camp

Zhejiang Hengdian Apeloa, headquartered at the Hengdian Center in Hangzhou’s Shangcheng District, operates as one of China’s leading pharmaceutical manufacturing companies. With seven API production facilities across Zhejiang province, the company delivers:

  • Chemical synthesis and fermentation capabilities
  • Contract development and manufacturing
  • R&D services with over 1,300 researchers
  • Regulatory-compliant manufacturing for global markets

From its base in Hangzhou to international offices in Japan, Germany and the USA, Zhejiang Hengdian Apeloa maintains its position as China’s second-largest API exporter while serving pharmaceutical markets worldwide.

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Detailed presentation of Main Camp

A leading pharmaceutical manufacturer in Hangzhou

Zhejiang Hengdian Apeloa, established in 1989, has grown into a major player in the pharmaceutical manufacturing sector. Based in the Shangcheng District of Hangzhou, the company operates under the Hengdian Group umbrella with over 7,000 employees worldwide.

Advanced facilities and capabilities

The company maintains seven manufacturing sites dedicated to active pharmaceutical ingredients, including five focused on chemical synthesis and two specialized in fermentation processes. Their cosmetic lab facilities are part of their extensive research and development infrastructure, supporting both pharmaceutical and cosmetic product development.

Research and development focus

With an R&D team exceeding 1,300 professionals and annual investment of over 5% of revenue, Zhejiang Hengdian Apeloa demonstrates its commitment to innovation. The company develops more than 15 new products annually for global regulatory submissions.

Global reach and market position

As China’s second-largest API exporter and a top 5 contract development and manufacturing organization (CDMO), the company maintains international operations with locations in:

  • Multiple sites across China
  • Tokyo, Japan
  • Frankfurt, Germany
  • Boston, USA

Quality and compliance standards

The company’s manufacturing facilities have successfully passed audits from major regulatory bodies since 2007, including:

  • NMPA (National Medical Products Administration)
  • US FDA
  • EMEA (European Medicines Agency)
  • PMDA (Pharmaceuticals and Medical Devices Agency, Japan)

Services and expertise

Operating from their Hangzhou headquarters, Zhejiang Hengdian Apeloa provides comprehensive services in drug development, biosynthesis, and chemical synthesis. Their product pipeline includes 50 products in various stages of development, serving pharmaceutical markets worldwide.

Services provided by Main Camp

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Frequent questions

Zhejiang Hengdian Apeloa operates in pharmaceutical manufacturing with these capabilities:

  • Active Pharmaceutical Ingredients (API)
    • Chemical synthesis products
    • Fermentation-based products
    • Biosynthesis development
  • Manufacturing Facilities
    • 7 API production sites
    • 2 drug product facilities
    • Quality control laboratories
  • Product Development
    • 15+ new products annually
    • 50 products in development
    • API export operations

The company maintains production standards according to international regulatory requirements.

Zhejiang Hengdian Apeloa operates in pharmaceutical manufacturing with these capabilities:

  • Active Pharmaceutical Ingredients (API)
    • Chemical synthesis products
    • Fermentation-based products
    • Biosynthesis development
  • Manufacturing Facilities
    • 7 API production sites
    • 2 drug product facilities
    • Quality control laboratories
  • Product Development
    • 15+ new products annually
    • 50 products in development
    • API export operations

The company maintains production standards according to international regulatory requirements.

Zhejiang Hengdian Apeloa operates in pharmaceutical manufacturing with these capabilities:

  • Active Pharmaceutical Ingredients (API)
    • Chemical synthesis products
    • Fermentation-based products
    • Biosynthesis development
  • Manufacturing Facilities
    • 7 API production sites
    • 2 drug product facilities
    • Quality control laboratories
  • Product Development
    • 15+ new products annually
    • 50 products in development
    • API export operations

The company maintains production standards according to international regulatory requirements.

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