5th International Conference on Pharmaceuticals, API and Manufacturing

"Enabling Technologies for API, Formulation and Manufacturing"

15th - 16th March 2019, Jakarta, Indonesia

Call For Abstract

  1. Synthesis aspects of an API
  2. Formulation aspects of an API
  3. Regulatory aspects of an API
  4. Scale up and Manufacturing aspects of an API
  5. Intellectual property aspects of an API
  6. Quality and testing aspects of an API
  7. Polymorphism aspects of an API
  8. Impurities Synthesis aspects of an API
  9. Process development of an API
  1. Pharmaceutics and Drug Delivery
  2. Pre Formulation & Formulation Aspects
  3. Preformulation in Drug Development
  4. Major Challenges in Drug Development
  1. Recent trends in Drug Discovery and Development
  2. Analytical strategies for pharmaceutical products
  3. Drug Prices and Consumer Value in R&D
  4. Pharmacoeconomics and pharma market research
  5. Stability of drugs
  1. Computer Aided Drug Design
  2. Drug designing and Molecular Modelling
  3. Clinical Trails and Regulatory Affairs
  4. Drug Design Software
  5. Medicinal Chemistry in Drug Discovery
  1. Regulation of Pharmaceutical Excipients
  2. Excipients used in Oral-Liquid formulations
  3. Excipient Interactions
  4. Emerging excipients in Parenteral Medications
  5. Excipients Quality Assurance
  1. Challenges to Pharmaceutical Nanotechnology
  2. Nanotechnology in Drug Delivery
  3. Pharmaceutical Nanotechnology based Systems
  4. Cellular and Sub cellular Nanotechnology
  5. Advancement In Nanotechnology
  1. Parental Formulations
  2. Topical Formulations
  3. Oncological Formulations
  4. Modified release Formulations
  5. Novel Drug Formulations
  1. Bioavailability and Bioequivalence perspectives for Drug Products
  2. In vitro-In vivo correlation
  3. Bioequivalence Study Design
  4. Drug-release studies
  1. Analytical Techniques for the development of new drugs
  2. Chromatography and Separation Techniques
  3. Advanced techniques for validation
  4. Drug Evaluation Methods for Pharmaceuticals
  5. Market Analysis for Pharmaceutical products
  1. Bioavailability and Bioequivalence perspectives for Drug Products
  2. In vitro-In vivo correlation
  3. Bioequivalence Study Design
  4. Drug-release studies
  1. Advancements in Parenteral Drug Delivery Systems
  2. Pharmacokinetic profiles
  3. Patient compliance
  4. Modified release Formulations
  1. Drug Delivery and Device Development
  2. Routes of Drug Delivery
  3. Drug-Device Combinations
  4. Inhalation drug delivery devices
  5. Biopolymers in Drug Delivery
  1. Drug Safety
  2. Best Industry Practices
  3. Current GMP Guidelines (cGMP) & GxP in Pharmaceuticals:
  4. Best Industry Practices
  5. Regulatory Strategies and developments for new drugs
  6. Regulatory Requirements for Pharmaceuticals
  7. Pharmacoeconomics & outcomes research
  8. Biosimilars

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