Our Services
Comprehensive pharmaceutical, drug innovation, and clinical research solutions designed to meet international standards of quality and efficacy.
Pharmacy Services
We deliver a full spectrum of pharmacy services — from hospital formulary management to patient-focused counseling — ensuring that every patient receives safe, effective, and affordable medication.
- Licensed and DRAP-certified pharmacy operations
- Automated dispensing with barcode verification
- Integrated hospital pharmacy management systems
- Cold-chain handling for biologic medications
Retail & Hospital Pharmacy
Full-service pharmaceutical dispensing for hospitals, clinics, and retail chains with automated systems ensuring accuracy and safety.
Drug Distribution & Logistics
Cold-chain capable distribution networks ensuring drug integrity from manufacturer to patient across Pakistan.
Patient Counseling
Dedicated pharmacist consultations helping patients understand medication regimens, interactions, and adherence strategies.
Medication Management
Comprehensive medication therapy management (MTM) programs for chronic disease patients and complex therapeutic regimens.
Drug Innovations
Our drug innovation division is at the forefront of pharmaceutical R&D, developing next-generation therapies that address unmet medical needs in Pakistan and global markets.
- Advanced drug delivery system design
- GMP-compliant manufacturing scale-up
- Stability studies and shelf-life optimization
- Intellectual property and patent support
Novel Formulation Development
From concept to prototype, we design advanced drug delivery systems including extended-release, nanoparticle, and targeted formulations.
API Synthesis & Optimization
Scalable active pharmaceutical ingredient (API) synthesis with process chemistry optimization for maximum yield and purity.
Pre-Clinical Studies
Comprehensive in-vitro and in-vivo preclinical testing to evaluate drug safety, pharmacokinetics, and efficacy before human trials.
Regulatory Dossier Preparation
Expert preparation of CTD (Common Technical Dossiers) for DRAP and international submissions to fast-track approvals.
Clinical Research
Our clinical research organization (CRO) services span all phases of clinical development, delivering high-quality, submission-ready data that accelerates drug approval timelines.
- ICH-GCP certified clinical investigators
- Institutional Review Board (IRB) coordination
- DRAP IND/NDA submission support
- Real-time clinical trial monitoring
Phase I – IV Clinical Trials
Conducting all phases of clinical trials with rigorous protocol design, patient recruitment, and data integrity assurance.
Bioequivalence Studies
DRAP-compliant bioequivalence and bioavailability studies for generic drug development and market authorization.
Pharmacovigilance
Post-market surveillance and adverse drug reaction monitoring to ensure ongoing product safety after approval.
Data Management & Biostatistics
Comprehensive clinical data management, statistical analysis plans (SAPs), and regulatory-ready final study reports.
Looking for a Specific Service?
Our team is ready to tailor solutions to your unique pharmaceutical and research needs. Reach out to discuss how Ibraheem Corporation can support your goals.
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