Company Established in the year 1999, Are one of the prominent processors and suppliers of a wide range of Intravenous Fluids and other high value Pharmaceutical Formulations. We are offering our clients LVP (Large Volume Parenteral s) and SVP (Small Volume Parenteral s). The company has been granted a license by Food and Drug Administration ( Madhya Pradesh) Manufacturing for small volume parenteral and

About Author:
Dr. Vishwas B. Chavan
Ph.D. (Biochemistry)
Andheri (East), Mumbai – 400069
vishwaschavan2003@yahoo.co.in

Abstract:
The word “Cancer” is still synonymous with death for common people and the “stage IV cancer”, which is typically known as “last stage cancer”, is loss of hope even for medical community.
Many times patient presents to clinic, when cancer had already crossed II^{nd or} III^rd stage. This is mostly due to the reason that cancer may not have any symptoms at initial stages. Even if there are any symptoms, they can be mild and vague. Further rising cost of healthcare forced many patients, particularly women, to delay approach to physician. Therefore it is not uncommon for cancer patients to hear sentences like, “You are too late”, “You should have come earlier” etc. which is more depressing. This is a humble attempt to give the these patients some ray of hope.
So, in this 21^st Century, is it necessary, that cancer should be equal to death all the times, even when it has reached stage IV? To get answer of this question, we need to first know what stage IV cancer is and what its effects on human body are.
As most people know, cancer or malignancy means uncontrolled growth of any cell of the body. The mechanism which controls the growth of cells is lost in malignant cells. Cancer can occur in any cell of body and hence any organ can be affected by cancer, though cancers of some organs are more prevalent in some populations.

About Author:
Kapil Tomer
Assistant Professor of Law
IMIRC College of Law
Garh Mukteswar, Panchshell Nagar (Ghaziabad)
kpltomer75@gmail.com

ABSTRACT
In the modern age, we are now living with increasing stress owing to various factors. In the times to come, the stresses and strains will be further cared out, thereby making mental health a very significant issue. According to NIMHANS (National Institute of Mental Health and Neuro Sciences), there are over two crore persons in our country who are in need of treatment for serious mental disorder and about five crore people who are affected by common mental disorder.

Applications invited for post of Drug Inspector Gr B by online method.

Post : Drug Inspector

We are 5th largest pharma co. of India and going to launch OPHTHALMIC DIVISION at India level and we require more than 200 MEDICAL REPRESENTATIVES in different locations of India.

Post: Medical Representative [ Ophthalmic division ]

The company "Evolet Healthcare” specializes in providing outsourcing services in the field of contract manufacturing of pharmaceutical products. The company was founded by professionals with extensive experience in manufacturing and marketing of pharmaceutical products.

Post: Regional Sales Manager

Application for filling up of temporary position of JRF / Project Assistant on contract basis Applications are invited on plain paper for filling up temporary position of JRF / Project Assistant II on contract basis, as per the following details:

Post: JRF / Project Assistant

National Institute of Pharmaceutical Education and Research (NIPER) is the first national level institute in pharmaceutical sciences with a proclaimed objective of becoming a centre of excellence for advanced studies and research in pharmaceutical sciences. The Government of India has declared NIPER as an ‘Institute of National Importance’.

Columbia Institute of Pharmacy is promoted by Janpragati Education Society (JPES). It is managed by a duly constituted Governing body. The Pharmacy institute was established in 2004-05. The motto was to impart value based education in the field of pharmacy. Here efforts are made to craft such health care professionals who would provide exemplary services for the welfare of mankind.

About Authors:
Lohithasu Duppala* , Manikumar Kothakota
GITAM Institute of Pharmacy,
GITAM University, visakhapatnam, Andhra Pradesh, India-530045.
* lohithasu@gmail.com, +919491894432

INTRODUCTION:
Cell Theory:
· All organisms consist of one  or more cells.
· Cell is the smallest unit of life.
· All cells come from pre-existing cells.

Cell cycle:
The dividing and non –dividing stages in the life of a cell are described by a series of events called the cell-cycle. The cell cycle  is the sequence of events by which a cell duplicates its genome and divides into daughter cells.Some cells, like skin cells ,divide continuously throught the life of the organism.Cardiac muscle cells are arrested in G2 phase.

About Authors:
Sharma Monish*, Kumar Bhupender
Seth G.L Bihani S. D. College of Technical Education,
Institute of Pharmaceutical Sciences & Drug Research.
Sri Ganganagar, Rajasthan (INDIA)
*monish28sharma@gmail.com

Introduction :
The name “Allium sativum” is derived from the Celtic word “all”, meaning burning or stinging, and the Latin “sativum” meaning planted or cultivated. The English word, garlic, is derived from the Anglo-Saxon “gar-leac” or spear plant, referring to its flowering stalk.(Kemper J Kathi.2000)
Garlic (Allium sativum), a member of the Liliaceae family, is a common food for flavour and spice  and it is one of the herbs most commonly used in modernfolkloric medicine. Garlic was an important medicine to theancient Egyptians as listed in the medical text Codex Ebers(ca.1550 BC) especially for the working class involved in heavy labour because it was an effective remedy for many aliments such as heart problems, headache, bites, worms and tumours. In 1858, Pasteur noted garlic’s antibacterial activity, and it was used as an antiseptic to prevent gangrene during World War I and World War II. (Thomson Martha.et.al.2007, Tattelman Ellen.2005)

Advertisement for engagement in the post of Pharmacist on contractual basis . Applications are invited from eligible candidates in the prescribed format for selection to the above post under the control of Collector-cum- Chairman, IRCS, District Br., Sambalpur.

Post: Pharmacist

26 years of successful presence in the pharmaceutical industry; Focused on manufacture of APIs, contract research and contract manufacturing
2 US FDA inspected manufacturing facilities
Over 400 DMFs worldwide; with a presence in over 85 countries
40,000 sq. ft. state-of-the-art R&D facility at Hyderabad
Over 1000 employees

Post: Sales Manager

ABOUT AUTHORS:
P.PRATHYUSHA*
Department of Pharmaceutics,
Raghavendra Institute of Pharmaceutical and Educational Research,
Anantapur, A.P, India.
* prathyusha2012@gmail.com

ABSTRACT
In the present investigation, an attempt was made to formulate the Oral Controlled Release Matrix Tablets of Glibenclamide in order to improve efficacy, reduce the frequency of administration, reduce dose related side effects and better patient compliance. Four formulations were prepared by wet granulation method using Ethyl cellulose and as a polymer in the ratio of 1:1, 1:2 and 1:4 and Conventional Tablets by using  Starch mucilage as a granulating agent. The formulated granules showed satisfactory flow properties. All the tablets formulation showed acceptable pharmaco technical properties and complied with pharmacopoeial standards. The tablets were evaluated for weight variation, hardness, friability, drug content and invitro dissolution studies. In- vitro release studies were carried out at pH1.2 for first 2 hrs followed by phosphate buffer at pH7.4 over a period of 12hrs using USP dissolution apparatus. F3 shows good initial release of 25.2% in 1 hr and may extend release of 96.8% in 12 hrs. Different release models like zero order, first order, higuchi, Hixson-Crowell and krosmeyer-peppas were applied to invitro drug release data in order to evaluate the drug release mechanisms and kinetics. Formulated matrix tablets were compared with conventional and marketed (diaonil 5mg) formulations. Matrix tablets with optimum concentration of Ethyl cellulose were successfully developed and evaluated.

ABOUT AUTHORS:
DEVENDRA SINGH¹*, PANKAJ KUMAR SHARMA¹, ROOHI KESHARWANI², Dr. UDAI VIR SINGH SARA^1
1Raj kumar goel institute of technology, Delhi-Meerut Road, Ghaziabad, India
²Chandra shekhar singh college of pharmacy, Kaushambi, Uttar Pradesh, India.
* devendrasingh.pisces@gmail.com

ABSTRACT:
Oral administration still dominates drug therapy and more than 60 % of marketed drugs are oral products. This type of drug administration is preferred due to its convenience, high patient compliance, less stringent production conditions and lower costs. Unfortunately, this traditional drug delivery method has its limitations, due to gastrointestinal permeability, metabolism and elimination of drugs by the liver or gastrointestinal mucosa (first-pass effect). The main drawback of the oral route is that only those compounds that are stable in the gastrointestinal tract can be administered in this way. For this reason, the oral route has been used for mainly non-peptide drugs. Delivery of a drug by oral route is predominantly restricted by pre-systemic degradation and poor penetration across the gut wall. The major challenge in the oral drug delivery is the development of novel dosage forms to endorse absorption of poorly permeable drugs across the intestinal epithelium. In this article we reviewed the various permeation enhancers, histology of small intestine, barriers, application, advantages, some basic permeability enhancement techniques which are useful for enhancing the permeability of poorly permeable drugs

The United States Pharmacopeia (USP) is a non–governmental, official public standards–setting authority for prescription and over–the–counter medicines and other healthcare products manufactured or sold in the United States. USP also sets widely recognized standards for food ingredients and dietary supplements.

Reputed Bangalore based company with 500cr turn over.

Post: Marketing Manager

CCRH, an autonomous body under the Department of AYUSH, Ministry of Health and Family Welfare, Government of India intends to engage the following categories of personnel on contract basis for a period of 06 (six) months for Homoeopathic Pharmacopoeia Laboratory (HPL), Ghaziabad (Uttar Pradesh).

The Indian Institute of Toxicology Research (IITR), established in 1965, a constituent laboratory of Council of Scientific & Industrial Research (CSIR) engaged in the Research & Development in the areas of Environmental Toxicology, Predictive Toxicology, Health Risk Assessment, Preventive Toxicology, Inhalation Toxicology, Analytical Toxicology, and also National S&T Missions. IITR has two campuses; the main campus is located at the centre of Lucknow City and the other campus at a distance of approx.