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16th World Congress on Industrial Pharma and Marketing (CSE)

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16th World Congress on Industrial Pharma and Marketing

About Euro Industrial Pharma

We are honored and delighted to welcome you to attend “16th World Congress on Industrial Pharma and Marketing” to be held in beautiful "city of lights" at Paris, France during May 13-14, 2019. The projected theme of the conference is “Transforming technology and its usage in pharmaceutical industry”.

Our ambition is to layout the bridge and enhance a network where our scientists, industry related researchers and contributors of related field can share their ideas, modern day research, their experience, associated problems, imaginative theories, frameworks, methodologies, tools, applications and questions throughout the scientific community. This conference provides the best opportunities to inspire and influence the largest assemblage of contributors from the field of industrial pharma.

This conference provides a platform that mainly focuses on pharmaceutical formulations, type of material used in pharmaceutical industry, contribution of technology in the field of pharma, novel drug delivery techniques, drug discovery, drug design and drug development, Challenges in pharma and marketing, research and development. Understanding the customer requirements, need of new strategies in pharmaceutical sector to grow eventually with time.

This conference comprises of various sessions including: special keynote sessions, panel discussions, and poster presentations, young researcher forums, E-posters conducted by the most outstanding and renowned speakers in the field of industrial pharmaceutical.

Sessions on Industrial Pharma Congress

Global Pharmaceutical industry
The pharmaceutical industry is responsible for the development, production and marketing of medications. The factors that affect the pharmaceutical market size include disease prevalence, drug affordability, consumer attitudes, government policies etc. In total pharmaceutical revenue had exceeded one trillion U.S. dollars. Thus, its immense importance as a global sector is inarguable. Current and ongoing changes in policies, social technology and environment factors are influencing the pharma market.
The global pharma market is expected to grow at a CAGR of 5.78% during 2017-2021 and is forcast to to be worth $1.170.4 billion by 2021.
Global Drug Market
The Drug market is segmented based on therapeutic area. The largest pharma market globally is for musculoskeletal drugs.The Segment is account for 14% of the total and as the largest segment worth $130.2 billion last year. These are the treatment for disease such as arthritis, tendonitis, osteoporosis.
Cardiovascular drugs are the second largest segment worth $129.6 billion followed by oncological drugs with worth125.9 billion. Ophthalmology drugs and anti-infective drugs are the smallest major segment.
Drugs for treating metabolic disorders such as will be the fastest growing segment of the pharma market to 2021.
Pharmaceutical drugs are subject to large number of laws and regulations that deal with patenting , testing, safety and marketing .These can act as barrier for small companies. Demand of generic drugs is increasing particularly in developing economies like China, India, Russia where government supporting their production in order to make lower-price treatments widely available.
Top pharmaceutical companies
Pfizer, GSK, Novartis, AstraZeneca, Sonafi, Gilead etc together top ten pharma companies account for 30% of the global sales.

Drug Discovery and Design
Drug discovery is the process through which potential new medicines are identified. Hot trends in pharmaceutical industry for drug discovery include Mass spectrometry drug discovery, Adoption of artificial intelligence, Targeting RNA with small molecules, Phenotypic screening and Organ-on-chips etc. Drug discovery involves wide range of scientific disciplines, including biology, chemistry and pharmacology. Drug discovery models in pharma industry are chemical approaches, genomic approaches, fragment based, CNS and cancer based drug discovery etc
Drug design is the inventive process of finding new medication based on the knowledge of a biological target. It involves the design of molecules that are complementary in shape and charge to the bimolecular target with which they interact and therefore will bind to it.
Computer-Aided Drug design (CADD)
Computer-assisted drug design
Structure-based drug design

Pharmaceutical Manufacturing
The process of drug manufacturing can be broken down into a series of unit operations, such as weighing and dispensing, milling, granulation, coating, tablet pressing, compression, blending and others. Production of bulk drug substances depends upon processes like fermentation (for production of antibiotics, steroids and vitamins), organic chemical synthesis (to produce drug substances with unique properties) and natural/biological extraction (metabolites isolation).
Activated carbon or charcoal is used in pharmaceutical and chemical industry primarily as an adsorbent to remove pollutants during drug manufacturing process,for the purification of raw materials, removal of organic impurities and proteins, intermediate products as well as as for the purification of final product. In industries activated charcoal is common ingredient in water filter system for the removal of active pharmaceutical ingredient.

Pharmaceutical Clinical Trials
Clinical trials are research studies that test how well new medical approaches work in people. This is the primary way that researchers find out if a new treatment, like a new drug or medical device is safe and effective in people or has less harmful side effects than the standard.
Clinical Trial Phases
Phase I trial: To judge safety and side-effects and to find the correct drug dosage.
Phase II trial: To judge the efficacy of drugs or device.
Phase III trial: To evaluate how the new medication works in comparison to existing medications for the same condition.
The drug-development process will normally proceed through all four phases over many years. If the drug successfully passes through Phases I, II, and III, it will usually be approved by the national regulatory authority for use in the general population.

Pharma Industry Architecture
Process Architects are the key players in the coordination of project design with engineering requirements and regulatory compliance. The improved architecture of pharmaceutical production plant can help to implement strategic objectives, processes, planning and controlling.
The pharma plant should be solid and safe, designed in such a way that operation areas should be illuminated and ventilated. Flammable or hazardous products first-aid facilities should be installed.
Installation of equipment’s for the regulation of temperature, humidity and air purity must be installed at right place.
Process Architects leads the data collection and initiate the documentation for the development of design. Good pharmaceutical manufacturing design should aim beyond integration to promote synergy between systems.

Pollution Control
Pharmaceutical Waste Management/ treatment has great importance because of Healthy related issues (Irritant, toxic, radioactive) and Safety related issues (flammable, reactive etc.).Treatment of industrial waste is very important because improper disposal may have an adverse effect on land and aquatic system. The failure or proper waste management and inability to reuse such materials result in depletion of natural resources.
The other main action for preventing drug pollution is to incinerate unwanted drugs rather than flushing or throwing them in the trash.
Environmental law and Regulations

Advanced Pharmaceutical Analysis Techniques
Pharmaceutical analytical techniques deal with different processes to identify or quantify a substance, the components of pharmaceutical solution or the determination of the structures of chemical compounds used in the formulation of pharmaceutical product.

Instrumental methods are generally preferred due to their high speed, selectivity, specificity, accuracy and simplicity of analysis. Any change in the properties of the system are detected by measurement of absorbance, refractive index, migration difference, charge to mass ratio etc. Methods includes are spectral methods (Like UV spectroscopy, NMR flourimetry), chromatographic methods ( HPLC, GLC, TLC etc) and electro analytical method.

Quality control and Quality assurance
QC department play key role in any pharma company. QC scientist test samples from all phases of a manufacturing or other handling process, with th goal of determining if the substances meets the requirements or standards. Quality will be checked in different stages: Raw material analysis, in process sample analysis and finished product analysis, sterility testing. The QC had two different division: wet analysis and instrumental analysis.
QA refers to the step-by-step process of examining whether goods and services meet specific quality, efficacy and safety requirements, as per their intended use. Pharmaceutical companies follow SOPs to achieve efficiency, quality output and uniformity of performance, while reducing miscommunication and failure to comply with industry regulations.

Pharma Digitalisation
Technology has become a key differentiator and digitalisation stands tall as the major differentiator. Digitalisation provides a platform for the organizations, especially the ones actively involved in the manufacturing, research and development. We can see visible benefits in the areas of se­cured collaborative research, Quality by Design (QBD), Modelling and simulation in process development besides analytics and visualizations. . Digitalization has already made inroads into sales and mar­keting and has made significant positive impact on business.
Digitalisation helps in improving collaboration between various elements. The combined framework of integrated instruments, specific software and standardized hardware, information technology and the internet brings greater visibility to R&D processes.

Pharma industry regulations and guidelines
Pharmaceutical regulations across the world play an important role in ensuring the safety and efficacy of the approved drugs. Food and Drug Administration (FDA) ensures that new drugs are rigorously tested for safety, efficacy and minimal side effects. They also make check on the drug prices. All aspects of the life-cycle of new drugs are regulated, from patent application to marketing approval, commercial exploitation, patent expiration. The aim is to maintain the standards of the drug at every step to cater for the patient population of each country.
GMP (Good Manufacturing Practice) is the part of quality management, which ensures that products are consistently produced and controlled according to the quality standards. GMP aimed primarily at managing and minimizing the raw material adulteration risks, to minimize the adulterations during production phase and to ensure the quality, safety and efficacy of products.

Pharmaceutical management and auditing
Pharmaceutical management combines the study of basics of pharmaceutical sciences with management, marketing studies, sales and other fields related healthcare industry. Pharmacists with expertise in specialized areas such as consulting, legal practice, drug information, poison control and pharmacy affairs are becoming more in demand as the profession evolves. Pharmaceutical Care Management Association Specialty drugs are frequently administered by medical professionals at higher-cost treatment sites such as hospitals, infusion centres and physician offices.
Pharmaceutical audit process, allowing an exact assessment of the company’s conformity performance. The elements and steps involve in the audit process may differ depending upon the type of audit required Goods Manufacturing Practice (GMP) or Good Clinical Practice (GCP) and its applied regulation standards. A pharmaceutical audit plan may include; documentation and record control, Manufacturing process and equipment, training, validation and qualification.
Pharmacoeconomic study evaluate the cost and effects of a pharmaceutical product. It is a sub- discipline of health economics and serve to guide optimal healthcare resource allocation.

Pharmaceutical packaging
Packaging and labelling are two vital requisite of the pharmaceutical and cosmetic industry. All the above the packaging and labelling is also important for maintain the product quality. Labels should be designed as such thet they remain in place invariant during distribution, supply and storage. The label should tell about the official product name, active ingredients, security labels, Holographic labels, sequential product number, embedded image, Hidden marks and printing, mass encoding(trace and track technology),Barcodes etc.
The pharmaceutical packaging market is constantly advancing and had experienced annual growth for at least ten percent per annum with the most other packaged goods, pharmaceuticals needs reliable and speedy packaging solutions that deliver a combination of product protection, quality, patient comfort and security need.

Pharma Marketing
Market access strategy can help pharma companies set their products apart and perhaps realize a preferred position on payer formularies at desired prices and reimbursement levels. To build a smart marketing network pharma companies are now beginning to see the value of partnering with service providers with deep knowledge, experience in a variety of regulatory environments and understanding of highly complex healthcare systems.
Pharma market intelligence is the most important thing to drive in strategy and success in the marketplace. Pharma market intelligence helps to achieve accelerated growth in the pharmaceutical market and transform to do business. It provide the real time information, trends, market analysis, provide highly accurate data that help to understand the market.

E-marketing or eBusiness
On Social Media most successful pharma brands on social are the ones that focus on sharing content around the values of the company and its customers, not just on product or brands. There are brands which uses the social media in smart way like Vitabiotics, which makes vitamin supplements uses social media to raise the awareness about health issues. Similarly Johnson and Johnson uses social media to share the company’s values (its focus on family).
The major benefit of ebusiness is that it makes medicine more accessible. Patients can set up an automatic system and regular shipping to their place. CVS and amazon are the leading online pharmacy and it is estimated that online prescription orders account nearly 23% of the $465 billion worth of the pharamceuticals sold in the US.

Challenges for pharmaceutical industry
Policy reform any changes to healthcare with new presidential administration will undoubtedly have an impact on the pharmaceutical industry. The challenge to the pharmaceutical industry will be to enforce change while maintaining steady market growth. Slowed market growth is one of the most worrying aspects of the pharmaceutical industry.
Regulations and approval by government agencies are difficult for all industries, but there is a lot of pressure on government agencies to have stricter controls on the pharma industry. Key areas of concern for companies are annual fees, drug approvals, advertising and marketing. Other challenges include Sustainability challenges, impact of pharmaceutical and personal care products in environment, more options for customer, sustainability packaging, green formulations and social impacts.
Development of environment friendly techniques and formulations.


Please contact the event manager Marilyn (marilyn.b.turner(at)nyeventslist.com ) below for:
- Multiple participant discounts
- Price quotations or visa invitation letters
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- Event sponsorship

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