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Recommended Conferences for Pharmaceutical Reverse Engineering

Pharmaceutical Reverse Engineering

As per available reports about 16 relevant journals 65 Conferences, 315 workshops are presently dedicated exclusively to Pharmaceutical reverse engineering and about 2 articles are being published on Pharmaceutical reverse engineering.

Reverse engineering is methods that is used in re-produce and re-design an existing product. By using this method, the design of product can be study and improve produce. The purpose of this method to increase the product capability. This project related with redesign and analyzes the mold for a bottlepack cap at Ain Medicare. To produce the mold, measurement must be taken at the product, and fiom the measurement the product can be draw in the 3D model. The product will be measured by using suitable equipment. The filling simulation process by using moldflowExpress is used to analyze the design. Then, the design of the core and cavity of the product is finalized. The process flow started with indentifiying the part following with measuring the dimensions at the product and the end was simulating the filling process on the mold by using simulations.

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Scope and Importance:

This is the main purpose that will be study. From the reverse engineering process, to produce the new pattern of the product it must apply the injection molding process the injection molding process is use to produce the bottle pack cap by making the core and cavity of the product before this. To making the reverse engineering product, it must follow the first step until the last step in the reverse engineering process Reverse engineering process is a unique technique that uses the existing entity information to produce a new entity that has some of same properties of the existing entity

Reverse engineering of a formulation can be made by means of public province information about the symphony of a drug product, and applying acquaintance and knowledge of formulation discipline to increase an approximation to the quantitative formula and likely manufacturing process. 
It is attainable to assessment the quantitative formulation from the qualitative formulation using the information and understanding of: 
• Formulation science
• The repercussion of chemical structure for the stability of the API
• Excipients; understanding their function, their restrictions, and their levels of use
• Pharmaceutical unit processes
• How these different facets of the product interact with each other

Market Analysis:

An overview of the global market for generic drugs, including coverage of therapeutics such as antibacterials, antidepressants, anticancer agents, anti-arthritics, cardiovascular drugs (e.g., hypolipidaemics and antihypertensives), and drugs for respiratory conditions, including asthma and COPD. The global generics sector reached $269.8 billion in 2012. This sector is expected to reach $300.9 billion in 2013 and $518.5 billion in 2018, with a compound annual growth rate (CAGR) of 11.5%.Analyses of global market trends, with data from 2012, estimates for 2013, and projections of compound annual growth rates (CAGRs) through 2018.

International symposium and workshops

1. Pharmacology 2016 sponsored by the British Pharmacological Society, December 13 - 15, 2016, London, United Kingdom

2. CPPM 2016 : International Conference on Pharmacology and Pharmaceutical Medicine, Feb 11-12, 2016 Kuala Lumpur, Malaysia

List of Best International Conferences:


  • Alphapharm 
  • AstraZeneca
  • Novartis
  • Roche
  • Merck & Co.
  • Sanofi
  • GlaxoSmithKline
  • Johnson & Johnson
  • Pfizer
  • Bristol-Myers Squibb
  • AbbVieVivisol

This page will be updated regularly.

This page was last updated on 31st Oct, 2015

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