Industrial Pharmacist Experts
Industrial pharmacists research drug compounds and flourish new medications based on research. They test medicines for efficiency and security, oversee the manufacturing process to ensure medications are produced accurately, and they engage marketing and promoting new drugs to consumers, hospitals and doctors' offices. An industrial pharmacist may also be pledged for conducting clinical trials and evaluating the outcome of these trials to gauge a drug’s effectiveness and to determine potential risks or side effects. As part of a clinical drug trial, industrial pharmacists collaborate with other pharmaceutical companies, local and federal governments, and a variety of health care professionals to ensure trials are conducted safety and within federal or state guidelines for drug testing. Pharmacists must have a Doctor of Pharmacy degree from an accredited college or university. To gain admission to a doctorate program in pharmacy, applicants must complete course work in anatomy and physiology, general biology, general chemistry, microbiology, organic chemistry, physics, immunology research, biochemistry, statistics, calculus, economics and the liberal arts. Pharmacists must be licensed by the state in which they intend to practice. Licensing requires successfully passing two comprehensive exams.
- Industrial Safety
- Industrial Regulations
- Industrial Design
- Pharmacy Management and Law
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Industrial Pharmacist Experts Conference Speakers
Recommended Sessions
- Clinical Studies
- Drug Design and Marketing
- Drug Development Stages
- Drug Discovery and Drug Development
- Functions of Regulatory Bodies
- Good Manufacturing Practices
- Healthcare Pharmacy
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- Industrial Pharmacy Management
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- Semi-Solid Dosage Forms - Formulations 2025 (France)
- Sexually Transmitted Bacterial Infections and Resistance Trends - Euro Antibiotics 2025 (Netherlands)
- Signal Prioritization and Management Techniques - Clinical Trials-2026 (UK)
- 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)