Call for Abstract
3rd International Conference and Exhibition on Pharmaceutical Development and Technology, will be organized around the theme “Pioneering the Development of Pharmaceutical Technology”
Pharmatech 2019 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in Pharmatech 2019
Submit your abstract to any of the mentioned tracks.
Register now for the conference by choosing an appropriate package suitable to you.
This track includes Pharmaceutical Formulation which is the process in which different chemical substances i.e., active chemical substances will combined together to produce a medical compound i.e., medical drug. This process involves production of drug which characterized by two things: Stability of the product, second Acceptability to the patient. Formulation studies focuses on factors like particle size, polymorphism, pH and solubility, in order to check whether these factors will effect on bioavailability of the drug or not. Pharmaceutical Formulations include Ophthalmic Formulation, Paediatric Formulation Development, Topical Formulation and Medication Formulation.
This track is representing Pharmaceutical Excipients Pharmaceutical Product Development ,Types of Drug Formulation ,Ophthalmic Formulation ,Pediatric Formulation Development, Medication Formulation ,Topical Formulations
- Track 1-1Pharmaceutical Excipients
- Track 1-2Pharmaceutical Product Development
- Track 1-3Types of Drug Formulation
- Track 1-4Ophthalmic Formulation
- Track 1-5Pediatric Formulation Development
- Track 1-6Medication Formulation
- Track 1-7Topical Formulations
Noticing drug targets plays essential roles in designing noval drugs and combating diseases. Unfortunately, our current knowledge about drug targets is far from comprehensive. Screening drug targets in the lab is an expensive and tedious procedure. In the past decade, the accumulation of various types of study of science related data makes it possible to develop computational approaches to predict drug targets.
This session represents Rational drug design Biotargets Computer Aided drug Design Bioweapons Tumor Targeting Mitochondrial Targeting
- Track 2-1Rational drug design
- Track 2-2Biotargets
- Track 2-3Computer Aided drug Design
- Track 2-4Bioweapons
- Track 2-5Tumour Targeting
- Track 2-6Mitochondrial Targeting
In the third track of ‘Pharmatech’ will be discussing about the Pharmaceutical Research that covers research spanning the entire spectrum of drug discovery, development, evaluation, and regulatory approval. Small drug molecules, biotechnology products which also includes genes, peptides, proteins and vaccines, and genetically engineered cells are an integral part of recent published papers.
- Track 3-1Small Drug Molecules
- Track 3-2Development of Vaccines
- Track 3-3Gene specific Drugs
- Track 3-4Proteins and Peptides
This session is of Pharmaceutical materials which are substances that are used in medical devices or in contact with biological systems. The Quality control and standardization of raw materials in pharmaceuticals has been a major step in the pre formulation studies of API’s, hence many recent pharmaceutical research organization have taken a step to overcome these aspects by thorough quality control techniques. Biomaterials use impression from medicine, biology, chemistry, materials science and engineering. Although biomaterials are primarily used for medical applications, they are also used to multiply cells in culture, to assay for blood proteins in the clinical laboratory, in proceeding biomolecules in biotechnology, for the regulation of fertility of implants in cattle and in diagnostic gene arrays and as well as in the adequacy of oysters and for investigational cell-silicon "biochips." The commonality of these applications is the interaction between biological systems and simulated or modified natural materials.
This term is represents the materials like Biomaterials Exfoliated Vermiculite Polymers Graphene Quantum Dots Microcapsules Hybrid materials
- Track 4-1Biomaterials
- Track 4-2Exfoliated Vermiculite
- Track 4-3Polymers
- Track 4-4Quantum Dots
- Track 4-5Graphene
- Track 4-6Microcapsules
- Track 4-7Hybrid materials
This session of Pharmaceutics and Bio pharmaceutics concerned with all Advancement and Development of Pharmaceutics and Bio pharmaceutics. Bio pharmaceutics examines the inter relationship of the physical/chemical properties of the drug, the dosage form (drug product) in which the drug is given, and the route of administration on the rate and extent of systemic drug absorption. Pharmaceutics concerns with manufacture of drugs vaccines biological medical devices equipment and their design and validation. This also includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials.
- Track 5-1Physical pharmacy
- Track 5-2Pro-drug design
- Track 5-3Biologics
- Track 5-4Pharmaceutical Analysis
- Track 5-5Pharmaceutical Packaging
- Track 5-6Drug Pharmacokinetics
- Track 5-7Quality control
- Track 5-8Good Manufacturing Practices
The term is Pharmaceutical Biotechnology which is the branch of science that deals with all the technologies required for manufacturing, producing and registration of biological drugs. Pharmaceutical Biotechnology is an increasingly essential area of science and technology. The Pharmaceutical Biotechnology is largely spread area , ranging from many ethical issues to changes in healthcare practices and a significant contribution to the development of national economy. Biotech drug makers mainly use those microorganisms or highly complex proteins from genetically-modified living cells as components in medications to treat various diseases and conditions, from cancer to rheumatoid arthritis to multiple sclerosis.
This session includes Microarray Technology, Industrial Biotechnology ,Bio formulations, Vaccines and Antibiotics ,Nucleic Acid Products ,Biologically inspired Pharmaceutics
- Track 6-1Microarray Technology
- Track 6-2Industrial Biotechnology
- Track 6-3Bioformulations
- Track 6-4Vaccines and Antibiotics
- Track 6-5Nucleic Acid Products
- Track 6-6Biologically inspired Pharmaceutics
This term Nano pharmaceuticals gives an ability to identify the diseases at very earlier stages and the diagnostic applications can build upon the conventional procedures using nanoparticles. Nano pharmaceuticals is considered as an emerging field where the sizes of the drug molecule or a therapeutic delivery system works at a Nano scale. In the pharmaceutical industry, a never ending issue is the difficulty of delivering the appropriate dose of a particular active medication to specific diseased site. Nano pharmaceuticals have enormous potential in addressing this failure of traditional therapeutics which offers site-specific targeting of active agents.
- Track 7-1Nanomedicine
- Track 7-2Biomedical Nanotechnology
- Track 7-3Nanotechnology and Nanomedicine
- Track 7-4Nano Drug Delivery
- Track 7-5Nano Liposomes
- Track 7-6Nano Pharmaceuticals
- Track 7-7Applied Nanotechnology
This session is of Pharmaceutical technology which is the application of scientific knowledge or technology to pharmacy, pharmacology, and the pharmaceutical industry. It describes techniques , designs, and instrumentation in the preparation, compounding, manufacturing, packaging, dispensing and accumulating of narcotic and other preparations used in diagnostic and determinative procedures and in the treatment of patients.
This track represents Technology Transfer Pharmaceutical Technology Assessment Quality assurance Bioinformatics and Computational Biology Pharmacological Technology advances Pharmaceutical Packaging and labeling
- Track 8-1Technology Transfer
- Track 8-2Pharmaceutical Technology Assessment
- Track 8-3Quality assurance
- Track 8-4Bioinformatics and Computational Biology
- Track 8-5Pharmacological Technology advances
- Track 8-6Pharmaceutical Packaging and labeling
In this track of ‘Pharmatech’ will be discussing about Drug manufacturing (Pharmaceutical Manufacturing)which is a process of industrial-scale manufacture of pharmaceutical components by pharmaceutical companies. The process of pharmaceutical manufacturing can be broken down into a various steps of unit operations, such as granulation, coating, milling, tablet compressing, and others. Start-up Pharmaceutical Companies, drug manufactures, contract pharmaceutical companies, pharmaceutical marketing agencies all play a major role in drug manufacture from its raw material to the final finished product.
This track is representing Active Pharmaceutical Ingredient synthesis Processing and Engineering Medication management Bioprocessing Molecular isotopic engineering Supply chain safety
- Track 9-1Processing and Engineering
- Track 9-2Medication management
- Track 9-3Bioprocessing
- Track 9-4Molecular isotopic engineering
- Track 9-5Supply chain safety
- Track 9-6Pharmacy Compounding and Dispensing
- Track 9-7Active Pharmaceutical Ingredient synthesis
The term Pharmaceutical Engineering is a branch of science and technology that mainly involves the pharmaceutical science that deals with the development and manufacturing of components, products, and processes in the pharmaceutical industry. While developing a drug involves several interrelated disciplines, the particular subfield of "pharmaceutical engineering" has emerged recently as a distinct engineering discipline. This now helps in solving the problems by bringing the principles and quantitative training of engineering to complement the other scientific fields that are already involved in drug development.
This term represents various engineering principles like Pre formulation Freeze Drying techniques Pharmaceutical sales Pharmaceutical Process Equipment GMP International standards Pharmaceutical validation.
- Track 10-1Pre formulation
- Track 10-2Freeze Drying techniques
- Track 10-3Pharmaceutical sales
- Track 10-4Pharmaceutical Process Equipment
- Track 10-5GMP International standards
- Track 10-6Pharmaceutical validation
This term Drug Delivery Technology is one of the unprecedented progresses of pharmaceutical nanotechnology during the past few decades, the conventional drug delivery systems (DDSs) have been involved into smart DDSs with stimuli-responsive characteristics. To increase their therapeutic efficacy and reduce the related side effects, active drug molecules should selectively accumulate in the diseased site for a prolonged duration with high controllability. In comparison to the conventional DDSs, the smart controlled DDSs can effectively reduce the dose frequency, while maintaining the drug concentration in targeted organs/tissues for a longer duration. In this case, the controlled DDSs provide wide insights and fascinating properties for decreasing the drug concentration fluctuation, reducing drug toxicities and improving therapeutic efficacy.
In this track of “Pharmatech” we discuss about Instruments , apparatus, tools , software, material or other article, whether used alone or in combination used specifically for diagnostic or for therapeutic purposes and necessary for its proper application, intended for the purpose of diagnosis, prevention, monitoring, treatment or alleviation of disease are medical devices.
The term medical devices includes Biomedical Instrumentation Measurements 3D printing of medical devices Instrumentation for Psychophysiological Measurements Instrumentation for the Experimental Analysis of Behavior Pacemakers and Defibrillators Ophthalmic and ENT Instruments Computed Tomographic Scanning (CT Scanning) Positron-Emission Tomographic (PET) Scanning Thermography and Tomography Elastography and Ultrasonography Respiratory Therapy Equipment Instrumentation for the Medical Use of Radioisotopes Forensic Devices
- Track 12-1Biomedical Instrumentation Measurements
- Track 12-23D printing of medical devices
- Track 12-3Instrumentation for Psychophysiological Measurements
- Track 12-4Instrumentation for the Experimental Analysis of Behaviour
- Track 12-5Pacemakers and Defibrillators
- Track 12-6Ophthalmic and ENT Instruments
- Track 12-7Computed Tomographic Scanning (CT Scanning)
- Track 12-8Positron-Emission Tomographic (PET) Scanning
- Track 12-9Thermography and Tomography
- Track 12-10Elastography and Ultrasonography
- Track 12-11Respiratory Therapy Equipment
- Track 12-12Instrumentation for the Medical Use of Radioisotopes
- Track 12-13Forensic Devices
- Track 12-14Devices used in Colonoscopy
The term Regulatory affairs is a profession within regulated industries. Regulatory affairs have a very specific meaning within the healthcare companies. Regulatory affairs is a new profession which is developed from the desire of governments to protect the public health by controlling the efficacy and nature of the products in the fields such as pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines. Regulatory Affairs is involved in the development of new medicinal products from early on, by integrating regulatory principles and by preparing and submitting the relevant regulatory dossiers to health authorities.Regulatory Affairs is involved in every step of the development of a noval medicine and in the post-marketing activities with medicinal products.
This track is representing Regulatory & Pharmacovigilance Regulatory compliance Regulatory requirements of pharmaceutical products Marketing Authorizations Clinical Affairs & Regulatory Strategies Intellectual Property Rights
- Track 13-1Clinical Trials & Pharmacovigilance
- Track 13-2Regulatory compliance
- Track 13-3Regulatory requirements of pharmaceutical products
- Track 13-4Marketing Authorizations
- Track 13-5Clinical Affairs & Regulatory Strategies
- Track 13-6Intellectual Property Rights
This session of “Pharmatech” focusses on Pharmaceutical Management which is learning about the management and business angle of the health care and the pharmaceutical industry. It gives a strong focus on the basic sciences, combining biological and pharmaceutical sciences with general management studies and marketing.
Pharmaceutical management professionals make financial and business decisions regarding the research and development of noval medicine, marketing, and sales. They take decisions about which types of medication should be developed and how they will be marketed to the public once they have been approved by the Food and Drug Administration(FDA).