Excellence through qualification

We uphold the highest standards of pharmaceutical manufacturing by combining decades of experience and advanced technologies in our state-of-the-art facilities.

We source active pharmaceutical ingredients (APIs) and materials from a global network of highly qualified suppliers to ensure compliance with the most stringent quality, ethical, and regulatory requirements.

  • Full compliance

    EU GMP, WHO GMP, ISO
    GCC / SFDA, IQ, MOHAP
    … and other regional standards

  • 0

    Trusted suppliers

Drug manufacturing

Oral solid dose (OSD)

  • Tablets and minitablets
  • Capsules
  • Powder / granules
  • Lozenges

Our expertise extend to B-Lactam, controlled substance and broad-spectrum antibiotics​.

Sterile Formulations 

  • Parenteral solutions (aseptic /terminal filling)
  • Vaccines
  • Lyophilization
  • Sterile BFS solutions
  • 0

    Bulk manufacturing sites

  • 0

    Million units
    (OSD annual capacity)

  • 0

    Million units
    (Sterile Formulations annual capacity)

Primary packaging

Packaging 

  • Empty Ampoules |2-30ml
  • Empty Vials | 2-30ml

Packaging capabilities

Oral solid dosage (OSD):

  • Blister packs
  • Bottles

Parenteral:

  • Ampoules | 1ml – 30ml
  • Lyophilized (lyo) ampoules | 2ml – 30 ml
  • Vials | 2ml – 300ml
  • Lyophilized (lyo) vials | 2ml – 30ml
  • Pre-filled syringes (PFS) | 1ml – 20ml
  • Blow-Fill-Seal (BFS) | 2,5ml – 50ml
  • Cartridges | 1ml – 20ml

Secondary packaging

Standard Packaging
Outer cartons for blisters, bottles, and more primary packaging formats. Automated folding and insertion of patient information leaflets (PIL).

Non-standard Packaging
Semi-automated and manual solutions for special formats, including ampoules, vials, syringes, aerosols, inhalers, and respules.

Labelling
Customized labelling of cartons, bottles, and secondary units, including variable data (e.g., expiry, batch) and tamper evident solutions.

Serialization & Aggregation
Compliance-ready solutions for global track & trace regulations. Aggregation from unit to shipper level.

Artwork Management
Design, review, version control, and printing support for multilingual packaging components.

  • 0

    Packaging sites

  • 0

    Million packs
    (annual capacity)

  • 0

    Million empty ampoules and vials (annual capacity)

Supply chain and further services

Warehousing & Logistics

  • GMP-compliant storage (ambient & cold chain)
  • Distribution support and inventory management
  • Transport validation

Regulatory Support

  • Dossier preparation, validation and submission
  • Variation submission
  • CMC writing
  • Response documentation preparation

Quality Support

  • Full QP release and batch documentation
  • Additional QC services
  • Feasibility study and improvement

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