2024 - The Drug Development Process: An Intensive 2 Day Training Online

Join Top Drug Development Course To Shape Your Career!
The most successful among all courses for drug development, this course a World Compliance Seminars covers the most productive areas. It considers the worldwide market for the pharmaceutical industry along with other significant therapeutic areas. It also takes care of the professionals involved in the pharmaceutical industry. The course includes a wide spectrum of things and objectives that are necessary for everyone who enrolls for the best Drug Development Course. It includes the identification of drug targets and preparation of chemicals used in the making of drugs of various types. Furthermore, the experts take care of the developments in biologics, toxicity examination, clinic tests and examination, pre-clinical development, pharmacokinetics, and also pharmacovigilance. The process, thus, takes care of everything from the discovery of the drugs to post-marketing strategies. The developers involved in the process then explain all necessary aspects of the process of drug development.
This comprehensive course provides an in-depth exploration of the drug development process, from initial discovery through to market approval. Participants will gain a thorough understanding of each phase of drug development, including key scientific, regulatory, and commercial considerations. The course covers drug discovery techniques, preclinical and clinical trial design, regulatory requirements, and post-marketing surveillance. It is designed for professionals in the pharmaceutical and biotechnology industries, including scientists, researchers, regulatory affairs specialists, and project managers, as well as those seeking to enter the field.
2 Day Agenda
Presenting the Overview Of Drug Development Products
Explanation of product types and directions of administration
The comprehensive process of drug development
Definition and remedies involved in drug development
View on the global pharmaceutical and drug market
Global market shares of biological and chemical drugs
Role and responsibilities of professionals in drug development
Size and key therapeutic areas
Area-wise alterations
Drug discovery
Targets of the Drug in development
The Anthropological Genome Project
Lead compound recognition and optimization
Break
Supervisory submissions
Preparation of Common Technical Document
CTD components
Provincial managerial material
The application procedure for biologic and chemical drug products – US and EU
Break
Pre-clinical development
In-procedure controls and issue testing
Solubility, penetrability, and verbal bioavailability
Preparation decisions for refining bioavailability
Visual isomerism
Polymorph and salt form screening
Common formulation types
Clinical Research
Serious excellence qualities
Clinical education design
Methodical Increase Facts
Adversative incident reporting
Influence of mobile calculation on scientific investigate
Pharmacokinetics and toxicity Checks
Drug plasma absorption shapes
Preoccupation, delivery, absorption, and the abolition of drugs
First-pass absorption
Types of toxicity screening
Break 15 mins
Post-endorsement alteration
Difficulties regarding creation development
New ICH Q12 – the promise of relaxed post-sanction change
The present or existing situation
US and EU Pharmacovigilance Significant fundamentals of rule
Drug product creation
Delivery
ICH direction
Who will Benefit:
Medical and clinical investigators
Investigation & expansion scientists
Quality Assurance professionals
Scientific Research professionals
Auditors
Strategic planners
Senior sales managers
Regulatory Affairs Professionals
Non-scientific employees of pharmaceutical companies who would like to understand how drugs are developed
Regulatory affairs professionals
Project managers
CMC/pharmaceutical research professionals
Manufacturing Personnel
Newly-appointed staff with no previous experience in the pharmaceutical industry
Financial managers
Brand team personnel
Statisticians & data management professionals
A pharmaceutical employee who wishes to better their knowledge of drug development
Objectives of Learning:
Every participant in Drug Development Course can learn the following by the end of this course:
The construction of controlling submissions
How drugs are partitioned for noxiousness
Parts of dissimilar medicinal specialists
Issues moving oral bioavailability
Archetypal costs and timelines related to drug development.
The evidence obtained at each stage of scientific research.
How the safety and effectiveness of drug products are protected during QC announcement testing
How new drugs are developed against targets in the human body.
The potential influence of polymorphism, salt form, and isomerism on efficacy and safety
Details because drugs fail throughout the growth procedure
How formulation can affect drug performance
How the manufacture and distribution of drugs are measured