Super Generic drugs and Bio Betters
In order to improve investment returns the pharmaceuticals have started focusing on re-innovating in the form of value-added generics (Super Generics) and value-added biologics (bio betters). The Re-innovated product offers advantages in terms of patient convenience by new route of delivery, dosage form, pharmacokinetic profile, stability, efficacy, safety, process of manufacturing.
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Super Generic drugs and Bio Betters Conference Speakers
Recommended Sessions
- Acceptance of Generic Drugs by People
- Application of Quantitative systems pharmacology (QSP)
- Best Practices & Strategies for Generic Drug Development
- Bioequivalence approaches for complex injectable API and formulations
- Biosimilars
- Challenges of Manufacturing Generic Drugs
- Challenges of Marketing Generic Drugs
- Complex Generic Drug Product
- Current Good manufacturing practices (CGMP)
- Generic Animal Drug
- Modernization of Bioequivalence Standards for Generic Products
- Patent Access& Intellectual property& FDA Regulations
- Pharmaceutical Quality Assurance
- Quality by Design (QbD) for generic drugs
- Super Generic drugs and Bio Betters
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- Post-Marketing Surveillance and Phase IV Trials - Clinical Trials Congress-2026 (France)
- Pre-clinical and Clinical Trails - Pharmacology 2026 (Italy)
- Pre-Clinical and Clinical Trials - PHARMACOVIGILANCE 2026 (Italy)
- Precision Medicine - Personalizedmedicine-2026 (Switzerland)
- Precision Medicine and Biomarker Discovery - Clinical Trials Congress-2026 (France)
- Precision-Driven Chemical Innovation in Drug Development - PHARAMACEUTICAL CONF 2026 (France)
- Process Chemistry and Pharmaceutical Manufacturing - PHARMACEUTICAL CHEMISTRY 2026 (Italy)
- Public Health and Pharmaceutical Policy - PHARMA CONFERENCE-2026 (Spain)
- Purpose and Principles of GMP - PHARMACEUTICAL SCIENCES 2026 (Italy)
- QC & QA: Quality control and Quality assurance - MedTech-2026 (Switzerland)
- Quality Assurance (QA) in Clinical Trials - Clinical Trials Congress-2026 (France)
- Quality Assurance and Quality Control in Pharmaceutical Industries - Drug Safety 2026 (Italy)
- Quality Assurance, GMP & Biotech Manufacturing Excellence - PHARMA BIOTECH 2026 (UK)
- Quality by design (QbD) approach - MedTech-2026 (Switzerland)
- Quality Control and Analytical Method Development - Generic Drugs 2026 (UK)
- Quantitative Systems Pharmacology and Computational Modeling - Generic Drugs 2026 (UK)
- Quantum Chemistry in Drug Design - PHARAMACEUTICAL CONF 2026 (France)
- R&D Advancement: Road to New Medicines - PHARMACEUTICAL SCIENCES 2026 (Italy)
- Radiopharmaceutical Chemistry - PHARAMACEUTICAL CONF 2026 (France)
- Randomization in Trials - Clinical Trials Congress-2026 (France)
- Rational Drug Use and Medication Safety - clinical pharmacology 2026 (UAE)
- Real-World Evidence (RWE) and Real-World Data (RWD) - Clinical Trials Congress-2026 (France)
- Real-World Evidence in Clinical Trials - Clinical Research 2026 (UK)
- Real-World Evidence, Decentralized Trials & Emerging Technologies - EURO CLINICAL TRIALS 2026 (UK)
- Recent Advances in Pharmacology and Toxicology - Pharmacology 2026 (Italy)
- Recent Innovations in Pharmaceutical Technology - Clinical Trials Congress-2026 (France)
- Regenerative Medicine & Stem Cell Clinical Trials - EURO CLINICAL TRIALS 2026 (UK)
- Regulatory Affairs & Global Compliance in Clinical Trials - EURO CLINICAL TRIALS 2026 (UK)
- Regulatory Affairs and Drug Approval Systems - PHARMA CONFERENCE-2026 (Spain)
- Regulatory Affairs and Quality Assurance - Drug-Delivery-2026 (France)
- Regulatory Affairs, Quality Compliance, and Intellectual Property - PHARMACEUTICAL CHEMISTRY 2026 (Italy)
- Regulatory and Safety Toxicology - clinical pharmacology 2026 (UAE)
- Regulatory Authority Compliance - MedTech-2026 (Switzerland)
- Regulatory Compliance and Ethics - Clinical Trials Congress-2026 (France)
- Regulatory Frameworks and Global Guidelines for Generic Medicines - Generic Drugs 2026 (UK)
- Regulatory Guidelines and Global Compliance in Pharmaceuticals - Drug Safety 2026 (Italy)
- Regulatory Requirements for Pharmaceuticals - PHARMACEUTICAL SCIENCES 2026 (Italy)
- Regulatory, Quality Control, and Translational Aspects - Drug Devilvery 2026 (France)
- Reproductive and Developmental Toxicology - clinical pharmacology 2026 (UAE)
- Risk Assessment and Safety Evaluation in Drug Development - Drug Safety 2026 (Italy)
- Risk-Based Monitoring (RBM) - Clinical Trials Congress-2026 (France)
- Role of Digital Health and AI in Generic Drug Industry - Generic Drugs 2026 (UK)
- Role of Gut Microbiome in Cardiovascular Health - Cardiovascular-2026 (France)
- Role of Inflammation in Cardiovascular Diseases - Cardiovascular-2026 (France)
- Safety Pharmacology - Pharmacology 2026 (Italy)
- Semi-Solid Dosage Forms - Formulations 2026 (UK)
- Site Management Innovation - Clinical Research 2026 (UK)
- Site Selection and Management - Clinical Trials Congress-2026 (France)
- Smart Drug Delivery Systems - PHARMACEUTICA 2026 (UK)
- Smart Drug Delivery Systems - Formulations 2026 (UK)
- Smart Polymers and Biomaterials - Drug-Delivery-2026 (France)
- Solid Dosage Forms - Formulations 2026 (UK)
- Stem Cell and Genetic Clinical Research - Clinical Research 2026 (UK)
- Stereochemical Drug Design - PHARAMACEUTICAL CONF 2026 (France)
- Supply Chain and Distribution of Generic Medicines - Generic Drugs 2026 (UK)
- Targeted Oral and Gastro-Resistant Formulations - Drug Devilvery 2026 (France)
- Targeted Therapies - Personalizedmedicine-2026 (Switzerland)
- Targeted Therapies in Cardiovascular Regeneration - Cardiovascular-2026 (France)
- Targeting the Renin-Angiotensin-Aldosterone System (RAAS) - Cardiovascular-2026 (France)
- Technology in Pharma Sciences - MedTech-2026 (Switzerland)
- Telemedicine - Personalizedmedicine-2026 (Switzerland)
- Theranostics and Personalized Medicine - Drug Devilvery 2026 (France)
- Therapeutic Drug Monitoring - clinical pharmacology 2026 (UAE)
- Toxicology - Pharmacology 2026 (Italy)
- Transdermal and Intradermal Delivery Systems - Drug-Delivery-2026 (France)
- Transdermal and Topical Drug Delivery - Drug Devilvery 2026 (France)
- Translational and Precision Pharmacology - clinical pharmacology 2026 (UAE)
- Translational Research - Personalizedmedicine-2026 (Switzerland)
- Types of Formulations - Formulations 2026 (UK)
- Vaccine Delivery Technologies - Drug-Delivery-2026 (France)
- Vaccine Development and Immunopharmacology - Drug Safety 2026 (Italy)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2026 (UK)
- Vaccine Technologies & Immunotherapeutics - PHARMA BIOTECH 2026 (UK)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2026 (France)
- Wearable and Implantable Drug Delivery Devices - Drug Devilvery 2026 (France)