Active Pharmaceutical Ingredients
Active Pharmaceutical Ingredients (APIs) are the biologically active components in pharmaceutical products that produce the desired therapeutic effect. APIs can be synthetic or extracted from natural sources and must meet stringent quality and purity standards. API development involves chemical synthesis, purification, and characterization to ensure consistency and efficacy. APIs are the core component of drug formulations, and their quality is critical for the safety and effectiveness of medications.
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Active Pharmaceutical Ingredients Conference Speakers
Recommended Sessions
- Active Pharmaceutical Ingredients
- Analytical strategies for pharmaceutical products
- Bioequivalence and Bioavailability
- Clinical Pharmacy and Pharmacy Practices
- Clinical trials and Pharmacovigilance
- Drug discovery and NCEs
- Formulations and NNDS
- Novel Drug Delivery Systems, Biomarkers & Drug Targets
- Pharma Market Research
- Pharmaceutical Manufacturing and Pharmacoeconomics
- Pharmaceutical Manufacturing, Scale Up and Tech transfer
- Pharmaceutical Packaging and Logistics
- Pharmaceutical Sciences
- Pharmacoeconomics
- Pharmacogenomics and Pharmacoepidemiology
- Pharmacology and Toxicology
- QC & QA: Quality control and Quality assurance
- Quality by design (QbD) approach
- Regulatory Authority Compliance
- Technology in Pharma Sciences
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- Single-Use Technologies in Production - Biologics Meet 2026 (UK)
- Site Management Innovation - Clinical Research 2026 (UK)
- Smart Drug Delivery Systems - Formulations 2025 (France)
- Solid Dosage Forms - Formulations 2025 (France)
- Stem Cell and Genetic Clinical Research - Clinical Research 2026 (UK)
- Stewardship Programs in Human and Animal Health - Euro Antibiotics 2025 (Netherlands)
- Structure-Based Drug Design and Molecular Docking - Euro MedChem and CADD 2025 (France)
- Supply Chain Management - Pharmaceuticals-2025 (France)
- Sustainable Antibiotic Practices and Global Policy - Euro Antibiotics 2025 (Netherlands)
- Sustainable Biologics Manufacturing - Biologics Meet 2026 (UK)
- Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (France)
- Synthetic and Green Medicinal Chemistry - Euro MedChem and CADD 2025 (France)
- Systems Pharmacology and Drug Modeling - Euro Pharmacology 2025 (France)
- Target Identification and Validation - Euro MedChem and CADD 2025 (France)
- Targeted Drug Delivery and Nanomedicine in Infectious Diseases - Euro Antibiotics 2025 (Netherlands)
- Targeted Therapies - Personalizedmedicine-2025 (Switzerland)
- Technology in Pharma Sciences - MedTech-2025 (Switzerland)
- Telemedicine - Personalizedmedicine-2025 (Switzerland)
- The Role of CROs in Clinical Trial Execution - Clinical Trials-2026 (UK)
- Toxicological Impacts of Air and Water Pollution - Euro Pharmacology 2025 (France)
- Toxicology - Pharmacology 2026 (Italy)
- Toxicology and Safety Pharmacology - Pharmacology-2025 (Germany)
- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2026 (Italy)
- Vaccine Development Against Bacterial Pathogens - Euro Antibiotics 2025 (Netherlands)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Veterinary Pharmacology - Pharmacology-2025 (Germany)