About Conference
ConferenceSeries Ltd is a renowned organization that
organizes highly notable pharmaceutical
conferences throughout the globe. Currently we are bringing
forth “22nd International Conference and
Exhibition on Pharmaceutical Formulations” (Formulation 2019)
scheduled to be held during July 04-06, 2019 at Valencia,
Spain. The conference invites all the participants across
the globe to attend and share their insights and convey recent developments in
the field of Pharmaceutical Formulations.
Pharmaceutical Formulations 2019 has
everything you need:
Open panel discussions: Providing
an open forum with experts from academia and business to discuss on current
challenges in Pharmaceutical sciences, where all attendees
can interact with the panel followed by a Q&A session.
Speaker and Poster Presentations: Providing
a platform to all academicians and industry professionals to share their
research thoughts and findings through a speech or a poster presentation.
Editorial Board Meeting: Discussing
on growth and development of open access Pharmaceutical & Drug Development
Journals and recruiting board members and reviewers who can support the
journal.
Round Table Meetings: Providing
a platform where industry professionals meet academic experts.
Over 50+ organizations and international pavilions will
be exhibiting at Pharmaceutical Formulations 2019 Conference.
Exhibitors will include equipment manufacturers and suppliers, systems
providers, finance and investment firms, R&D companies, project developers,
trade associations, and government agencies.
In addition to the products and services you will have
access to valuable content, including Keynote Presentations, Product
Demonstrations and Educational Sessions from today’s industry leaders.
The Pharmaceutical Formulations 2019 has
everything you need, all under one roof, saving you both time and money. It is
the event you cannot afford to miss!CONFERENCE HIGHLIGHTS
Track 01: Pharmaceutical
Formulation
Pharmaceutical formulation is defined as the
process in which different chemical substances are combined to produce a final
medicinal product. Since 1991, we have been designing Liquid, Suspension,
Powder, Solid solution, Semisolid
formulations and even drug eluting devices. The formulation
studies involve developing a preparation of drug acceptable for patient. Pharmaceutical
Formulation is the word often used in a way that includes
dosage form. Formulation studies consider factors such as solubility, particle
size, polymorphism and pH as all of these can influence bioavailability and
hence the activity of a drug.
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Track 02: Solid Dosage
Forms
Solid dosage formulations are important dosage
forms in pharmaceuticals. e.g. tablets, capsules, granules, sachets,
reconstitutable powders, powders, dry powder inhalers and chewables. Solid dosage
form contains unit dose of one or more medicament. Easy to
package and carry around, solid dosage forms are also difficult to tamper with,
stable and easy to dose accurately – approximately 80% of errors in medication
are associated with the use of liquid
formulations. Excipients include Binders, Glidants, Sweeteners etc.,
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Track 03: Semi-Solid
Dosage Forms
Semi solid dosage forms are the
products when applied to the skin treat a pathological
condition and protects from other harmful environment. They are
smooth, non-staining and get miscible with skin secretions. Creams, Gels,
Pastes etc. are the examples. Semisolid dosage forms usually are intended for
localized drug delivery. In the past few years, however, these forms also have
been explored for the systemic delivery of various drugs. Semisolid dosage
forms for dermatological drug therapy are intended to produce
desired therapeutic action at specific sites in the epidermal tissue.
Track 04: Liquid Dosage
Forms
Liquid dosage forms are essential
Pharmaceutical products which involves a mixture of active drug
components and nondrug
components (excipients). Liquid dosage forms are prepared: a)
by dissolving the active drug substance in an aqueous or non- aqueous (e.g.
glycerin, ether, alcohol) solvent b) By suspending the drug in appropriate
medium or c) By incorporating the drug substance into an oil or water phase.
Ex: Suspension, Emulsion, Syrups, Elixers
Track 05: Gaseous Dosage
Forms
Gaseous dosage
forms are packed in a container which gets released upon
applying pressure. The gas inside contains therapeutically
active medicaments. The containers have valve systems with
continuous or limited delivery. They are used for topical application on skin
and as local application into nose and mouth. Ex: Nebulizer, Sprays,
Inhalers, April 11-13, 2017 Seoul, South Korea.
Track 06: Types of
Formulations
Formulations are
classified into two types: based on Route of
administration and Physical form. Based on route of
administration they are classified as Oral, Topical, Rectal, Parenteral,
Vaginal, Inhaled, Ophthalmic and octic. Formulation studies involve developing
a preparation of the drug which is both stable and acceptable to the patient.
For orally administered drugs, this usually involves incorporating the drug
into a tablet or a capsule. It is important to make the distinction that a
tablet contains a variety of other potentially inert substances apart from the
drug itself, and studies have to be carried out to ensure that the encapsulated
drug is compatible with these other substances in a way that
does not cause harm, whether direct or indirect.
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Track 07: Novel Drug
Delivery Systems
“Novel Drug delivery System (NDDS) refers to
the formulations, systems and technologies for transporting a
pharmaceutical compound in the body as it is needed to safely achieve its
desired therapeutic
effects. Drug delivery
systems (DDS), are based on approaches that are
interdisciplinary and that combine pharmaceutics, bio conjugate chemistry, and
molecular biology.
Track 08: General
Considerations in Dosage Forms
Prior to formulation some physico chemical
properties are characterized. Chemical properties include
structure, form and reactivity. Physical properties include particle size,
melting point and solubility. In case of some drugs biological
properties are also characterized. Age and sex of the patient
also play a major role in dosage design. The others factors are Solubility,
Buffer capacity and partition coefficient.
Track 9: Drug Formulation
Procedures
The drug subjected to drug development undergoes
number of trials and are screened at different stages to produce a final potent
drug for the treatment of various diseases. During this process different
properties are checked to see whether the drug is non-toxic to living system
and is therapeutic or not. Using suitable excipients and
technological preparations the active substances are formulated into final
dosage form. The final product is the Actual composition of preparation,
manufacturing specification.
Track 10: Pharmaceutical
Excipients
Pharmaceutical
excipients are those substances other than
the prodrug which are included in the manufacturing process or are
contained in a finished pharmaceutical product dosage form. There are
many excipients.
Few of them include Antiadherents, Binders, Coatings, Colors, Flavours, Lubricants,
Preservatives, Sweeteners etc. Excipients are crucial to drug delivery within
the body. Generally, an excipient has no medicinal properties. Its standard
purpose is to streamline the manufacture of the drug product and ultimately
facilitate physiological absorption of the drug.
Track 11: Drug Design and
Development
Drug design, also known as rational drug
design, is the inventive process of finding new medications based on
the knowledge of a biological target. Drug design defines 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. Drug
development is the process of bringing a new pharmaceutical
drug to the market once a lead compound has been identified
through the process of drug discovery.
Track 12: Pharmaceutical
Analysis
Pharmaceutical
analysis is a branch of practical chemistry that involves a
series of process for qualification, purification, identification and
determination of a substance, separation of the components of a solution or
mixture, or determination of structure of chemical compounds. The sample to be
analysed is called as analyse. Pharmaceutical Analysis is an Analytical
Method used to determination the quality and quantity of the pharmaceutical
products. It also gives the information about the purity and safety
of the products. Briefly it can be described as it identifies, determines,
quantifies, purifies and separates the active compound from the mixture.
Track 13: Drug Product
Manufacturing
The drug product
manufacturing facility is designed to produce injectable in syringes or vials
in Grade A environment. Industries strive to improve product quality in today’s
competitive environment and as well reduce the production cost. Scaling up from
our development services to full scale commercial drug product manufacture or
transferring existing commercial products we can meet your commercial drug product
manufacturing requirements.
Track 14: Smart Drug
Delivery Systems
Targeted drug
delivery sometimes called smart drug delivery is a method of
delivering medication to a patient in a manner that increases the concentration
of the medication in some parts of the body relative to other parts in the
meantime reduce side effects/toxicity of payloads which are key factors for
improving patient
compliance.
Track 15: Pharmacists Role
in Patient Safety
Pharmacists can play a role helping patients
with chronic diseases have better medication at
correct time and get good clinical outcomes. They play a key role in
immunization services and identifying vaccine candidates. They Participate and
maintain a significant role in multidisciplinary patient care rounds. Patients
often make their own decisions about managing their medications. Pharmacists could
usefully serve as patient advocates, providing information that permits
patients to assess risk and enhance their autonomy.
Track 16: Regulatory
Affairs
Regulatory affairs are a new profession which
is developed by the governments to protect public health.
The main aim is controlling the safety and efficacy of products in areas
including pharmaceuticals,
veterinary medicines, medical devices, pesticides, agrochemicals and cosmetics.
Regulatory affairs also have a very specific meaning within the healthcare
industries.
Track 17: Pharmaceutical
Formulations Market
Pharma industries are showing increased
confidence in the growth of manufacturing in
the market. This turn around in the market is due to the potential which is
being driven by concerns of quality in some Asian markets and a marketed shift
in the drug development.
The primary reason behind this is an increased regulatory confidence in the
standards of manufacturing.
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Track 18: Entrepreneurs
Investment Meet
Entrepreneurs who are ready to invest and get
profit by working hard in the field of pharmaceutical
formulations will be happy by attending this meeting and make
their way a successful one by meeting intellectuals and experts who can make
their investment worthwhile. This platform will be the best one to make a shape
of your business.
Drug Formulation
Conferences SUPPORTING JOURNALS
International Journal of Drug Development & ResearchDrug Designing: Open AccessJournal of Developing DrugsJournal of Pharmaceutical Sciences & Emerging Drugs
For More Information, PS: https://formulation.pharmaceuticalconferences.com/