Home › Finished Dosage Manufacturing

What we do

Oral solids, with a specialism in modified release.

Modified-release pellet technology is the technical centre of the group. It is a demanding discipline, and it is the reason our formulation capability extends beyond straightforward generic tablet manufacture.

01

Technology

Where the specialism sits.

Modified-release pellets

Sustained-release and delayed-release pellet systems, including enteric and multi-phase release profiles, developed to a defined dissolution target rather than an approximate one.

Ready-to-fill pellets

Pellets supplied to other manufacturers for encapsulation or compression — a business line in its own right, and a useful proof that the technology travels.

Directly compressible granules

Granulations engineered for direct compression, reducing process steps and improving content uniformity for suitable molecules.

Taste-masked granules

Taste masking for molecules where palatability governs adherence — particularly relevant in paediatric and geriatric presentations.

02

Development services

From molecule to validated process.

Formulation developmentExcipient selection, release-profile design and prototype development against a target product profile.
Process developmentDefinition and refinement of the manufacturing process, including critical process parameters and control strategy.
Analytical methodsMethod development and validation to recognised pharmacopoeial standards, including dissolution method development for modified-release profiles.
Stability programmesStability studies under defined storage conditions, with reporting appropriate to the intended market.
Scale-upProgression from laboratory through pilot to commercial batch scale, with process robustness demonstrated rather than assumed.
Technology transferTransfer to a receiving site, including documentation, training and support through validation batches.
03

Therapeutic areas

Where the portfolio concentrates.

The group’s formulation experience is weighted towards chronic disease and long-term therapy — the categories where modified release matters most and where continuity of supply is most consequential for a patient.

  • Proton-pump inhibitors
  • Antiplatelet therapy
  • Alpha-blockers
  • Calcium-channel blockers
  • Antidepressants (SNRI)
  • Antifungals
  • Aminosalicylates
  • Diabetes & metabolic
  • Hypertension & cardiovascular
  • Thyroid disease
  • Epilepsy & neurology
  • Respiratory disease
  • Pain, fever & musculoskeletal
  • Gastrointestinal & supportive care
On anti-infectives. Antimicrobials are handled within stewardship frameworks. Availability and stewardship are not in tension — unreliable supply drives substitution and sub-optimal prescribing, which is precisely what stewardship exists to prevent.

Next step

Looking for a formulation partner?

Contract development, contract manufacturing and ready-to-fill pellet supply are all live business lines.