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Manufacturing

Manufacturing Capabilities

We manufacture wide range of dosage forms complying to USFDA standard.

  • SOLID ORAL DOSAGE FORMS (TABLETS, CAPSULES, POWDERS, SACHETS, PELLETS AND BEADS)
  • PARENTERAL DOSAGE FORMS (LIQUID AND LYOPHILIZED POWDERS)
  • COMPLEX GENERICS (MODIFIED RELEASE, BILAYER, MUPS AND OCAS)
MANUFACTURING FACILITIES

Malaysia

Our manufacturing facilities in Bandar Enstek offer robust business connectivity to the regional market due to the location of less than 5km away from Kuala Lumpur International Airport (KLIA).

Spread across more than 12 acres of land, the facilities are designed by internationally renowned European pharma engineering firm to meet strict regulatory requirement of USFDA, EMA, PIC/S and WHO.

GENERAL PHARMACEUTICAL MANUFACTURING FACILITY

SYNERGY

Synergy is a finished products manufacturing facility based in Bandar Enstek, Negeri Sembilan. The state-of-the-art manufacturing facility is the FIRST in Malaysia with cutting-edge technology for palletisation, Bilayer and MUPS.

  • Synergy is also PIC/S approved and Halal compliant GMP facilities.
  • It is the FIRST pharmaceutical manufacturing facility in Malaysia and the only in Southeast Asia with USFDA accreditation and will undergo GMP accreditation from EU and WHO Geneva.
  • An annual production capacity of 2 billion tablets and capsules.
  • Explore Our CMO
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ONCOLOGY FINISHED PRODUCTS MANUFACTURING FACILITY

CELSUS

Celsus is the FIRST fully-automated, high-containment (OEB5) Finished Products manufacturing plant in South-East Asia. Annually, Celsus has the capacity to produce 650Mn+ tablets & capsules.

  • The facility is PIC/S approved GMP facilities.
  • It is the FIRST facility in Malaysia to undergo GMP accreditation from USFDA, EU and WHO Geneva.
  • The facility complies to the highest safety and environmental standards of OSHA and USFDA.
  • Explore Our CMO
GENERAL PHARMACEUTICAL MANUFACTURING FACILITY IN UZBEKISTAN

SYNERGY II

Located in the heart of Uzbekistan's capital city of Tashkent, SYNERGY II was acquired as part of a long-term vision to Novugen's global presence. The facility has a capacity to cater to the whole CIS region and other neighbouring countries.

  • State-of-the-art facilities engineered to the highest quality & safety standards
  • Annual capacity of 1 billion tablets
  • Capable to produce various dosage forms like sachets, syrups, vials and other dosage forms.
Uzbekistan
ONCOLOGY FINISHED PRODUCTS MANUFACTURING FACILITY, PAKISTAN

CELSUS II

CELSUS II is the FIRST Oncology Finished Products manufacturing plant in Pakistan.

  • Capable to produce injectables and oral solid dosage forms.
  • Capacity to produce 125Mn tablets & capsules annually
  • Designed to meet GMP quality & safety standards of WHO Geneva.
Highest Quality Standards

Quality

Our obsession for quality drives the company to achieve the highest standards for our products and services. This is aligned with our strategy and business philosophy to comply to USFDA and EU requirements through our day-to-day operations.

Compliance Systems

Our regulations and compliance systems assure pre-qualification of material vendors. We operate with stringent in-process system that provide control over any changes and documentation.