Finished Dosage Forms, Generic Formulations & Regulatory Support
From formulation development and pilot stability studies to high-throughput commercial manufacturing, Cross Corporation delivers finished dosage formulations across 15 therapeutic categories and 7 versatile delivery formats.
15 Strategic Therapeutic Segments
We develop and manufacture products across a wide spectrum of essential, chronic, and specialty medical fields.
Generics & NDPS Formulations
High-value generic combinations and controlled narcotic / psychotropic drugs handled with full statutory NDPS protocols and export NOCs.
Anti-HIV & Antivirals
Proven antiretroviral regimens, first-line and second-line therapeutics, and fixed-dose combinations meeting WHO treatment guidelines.
Oncology
Chemotherapeutic agents, hormonal therapies, targeted generic molecules, and supportive oncology medications.
Vaccines & Biologicals
Temperature-controlled, high-integrity immunization solutions and biological preparations distributed with cold-chain protocols.
Critical Care
Emergency medical solutions, intensive care injectables, anaesthetics, and emergency resuscitation formulations.
Dermatology
Topical therapeutic creams, dermatological gels, barrier ointments, and specialty antifungal / antibacterial solutions.
Antiseptics & Disinfectants
Hospital-grade surgical scrubs, broad-spectrum antiseptic solutions, and environmental sanitizing agents.
Analgesics & Pain Management
Immediate and modified-release analgesics, anti-inflammatories (NSAIDs), and specialized neuropathic pain formulations.
Antibiotics
Beta-lactams, cephalosporins, macrolides, and fluoroquinolones formulated in strict compliance with cross-contamination segregation standards.
Anti-Malarial
Artemisinin-based combination therapies (ACTs) and prophylactic antimalarial regimens formulated for tropical and endemic zones.
Cardiology
Antihypertensives, beta-blockers, ACE inhibitors, lipid-lowering statins, and antiarrhythmic agents for long-term cardiovascular management.
Diabetology
Oral hypoglycaemic formulations, biguanides, sulfonylureas, DPP-4 inhibitors, and fixed-dose synergistic combination tablets.
Nephrology
Phosphate binders, electrolyte management solutions, and renal supportive pharmaceuticals for chronic kidney care.
Neurology
Anticonvulsants, neuro-protectants, anti-Parkinsonian agents, and central nervous system therapeutics.
General Care & Primary Health
Essential vitamins, minerals, multivitamin syrups, antipyretics, and primary healthcare medicines for broad institutional supply.
7 Versatile Dosage Forms Manufactured
Engineered with precision tooling, automated barrier packaging, and stability testing across global climatic zones.
Tablets
Film-coated, enteric-coated, sustained-release, dispersible, and bi-layer combination tablets manufactured on high-speed rotary presses.
Capsules
Hard gelatin capsules, vegetarian HPMC shells, and delayed-release pellet formulations packed with automated weight-sorting.
Syrups & Suspensions
Oral liquids, pediatric syrups, and stabilized dry powder suspensions processed in automated stainless-steel mixing tanks.
Creams, Ointments & Gels
Topical emulsions and transdermal gel formulations filled into aluminum or laminated barrier tubes under positive pressure.
Lozenges & Chewables
Palatable chewable formulations, pediatric chewables, and therapeutic medicated throat lozenges.
Effervescent Formulations
Rapidly dissolving effervescent granules and tablets produced in dedicated low-humidity environmental suites.
Dosage Sprays & Inhalation Puffs
Metered-dose inhalers (MDI), nasal sprays, and oral aerosol puffs calibrated for precise micro-gram delivery.
Inside Our GMP Manufacturing Operations
Explore actual operational areas from our verified manufacturing facility, engineered for GMP workflow segregation, cross-contamination prevention, and safety.
Area 01 • Facility Infrastructure
Manufacturing Facility – External View
Designed for efficient workflow, perimeter safety, and strict compliance with GMP standards. Reflects organized industrial operations and clean environmental separation.
Area 02 • Approved RM
Raw Material Warehouse (Approved RM)
Raw materials are received, identified, sampled, and stored under controlled conditions in designated approved and quarantine areas with strict traceability before release.
Area 03 • Analytical QC
Quality Control Laboratory (HPLC Section)
Double-door access system ensures controlled entry, minimizing contamination risks. High-performance liquid chromatography ensures assay potency and stability compliance.
Area 04 • Primary Packaging
Alu-Alu Blister Packing Line
Dedicated to high-protection cold-formed aluminum blister packaging for solid dosage forms, ensuring superior moisture, oxygen, and light barrier properties for long shelf-life.
Area 05 • Liquid & Solid Packing
Bottle Filling, Capping & Sealing Line
Integrated automated line performs accurate filling, secure induction capping, and proper tamper-evident sealing of bottles under controlled clean conditions.
Area 06 • Packaging Precision
Self-Adhesive Labeling Line
Applies regulatory labels accurately on primary containers with online optical batch coding, barcode verification, and expiry tracking complying with export requirements.
Area 07 • Quality Inspection
Manual Visual Inspection Area
Dedicated to 100% visual inspection of sealed blister packs to verify seal integrity, absence of pinholes, and flawless packaging prior to secondary cartoning.
Area 08 • Secondary Packaging
Secondary Packing & Verification Table
Manual and automated verification of package insert leaflets, carton batch numbers, tamper stickers, and shipper packing accuracy before warehouse transfer.
Area 09 • Palletized Units
Finished Goods – Palletized Units
Shrink-wrapped trays organized systematically on standardized pallets for physical protection, batch traceability, and rapid international container loading.
Area 10 • Logistics & Storage
Finished Goods Warehouse
Temperature and humidity-monitored warehouse for organized quarantine, approved storage, and batch-wise dispatch complying with Good Distribution Practices (GDP).
Area 11 • Cleanroom Corridor
Production Block Main Corridor
Provides controlled differential air pressure and organized movement of personnel and materials between segregated manufacturing suites to eliminate cross-contamination.
Comprehensive Regulatory Dossier Capabilities
We understand that obtaining marketing authorizations and product registrations from foreign Ministries of Health (MOH) is the single most critical gatekeeper to commercial supply.
Cross Corporation prepares complete regulatory documentation tailored to the specific guidance documents of the importing authority:
- • Certificate of Pharmaceutical Product (COPP): Issued under WHO certification scheme by State FDCA and CDSCO.
- • Method of Analysis (MOA) & Certificate of Analysis (COA): Validated analytical methods and batch release data.
- • Accelerated & Real-Time Stability Studies: Conducted in calibrated ICH stability chambers up to Zone IVb (30°C / 75% RH & 40°C / 75% RH).
- • CTD & ACTD Regulatory Dossiers: Module 1 through Module 5 documentation including Master Formulas, Process Validation, and Batch Manufacturing Records.
- • Controlled Drugs Compliance: CDSCO Export NOC, State FDCA allocations, and NDPS statutory documentation.
Request Technical Dossier or Quotation
Are you registering formulations in your local market? Reach out to our technical regulatory team to receive product dossiers, sample batches, and pricing schedules.
Contact Regulatory Department