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Vacancies for GM (QC/QA); Manager/Asst. Manager (QC/QA) at Comed - High Exp require

Comed was in 1986, when a team of experienced and energetic Pharma professionals decided to go big and to do something different and better than routine. A seed was sown: a beginning was made. These young, dynamic and experienced future leaders chose Baroda (Now called Vadodara), the Educational and Pharma capital of Gujarat (Western India) as their base, a choice which itself proved to be big contributing factor for growth.

Post: GM (QC/QA); Manager/Asst. Manager (QC/QA)

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Job as Marketing Representive and Sales Executives in Devita Healthcare - 8 posts

DEVITA HEALTHCARE, our company has started marketing in respected gujarat. our company has long vision and long goal to established good market. we believe in making relationship.
Currently we have vacancies in diabetic and cardiac segment.

Post: Marketing Representive and Sales Executives - 8 candidate required

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PREPARATION AND CHARACTERIZATON OF ACECLOFENAC LOADED TOPICAL EMULGEL

ABOUT AUTHORS:
Sharma Devendra L.*1, Dr. A.K.Seth1, Nirmal Shah1, Sachinkumar P Chauhan, Chintan Aundhia
1Department of Pharmacy, Sumandeep Vidyapeeth University,
At & Po Pipariya, Ta.- Waghodia, Dist. Vadodara-391760.
(Gujarat) India
*9009dev@gmail.com

ABSTRACT
The main purpose of this work was to develope a topical emulgel formulation of Aceclofenac. Aceclofenac drug loaded formulation with Tween 80 as surfactant and PEG 400 as co-surfactant was developed  for topical application. Phase behavior and solubilization capacity of microemulsion system were characterized. Pseudo ternary phase diagram were developed by taking different concentration of Tween 80 and PEG 400 and the surfactant mixture containing tween 80 and PEG 400 ratio of (4:1) shows maximum amount of water. With the increase of tween 80 concentration, microemulsion region area and the amount of water and oil solubilsed into the microemulsion system increases, however increase of PEG 400 concentration produce opposite effects. The micromulsion system was also investigated in terms of other characterstics such as particle size, zeta potential, dilution test, centrifugation, conductivity, pH measurement, viscosity, % assay and % transmittance. Aceclofenac, poorly water soluble drug displayed high solubility in a microemulsion formulation using Capmul MCM oil (2.5%), Surfactant mixture (45%) and water (52.5%). The prepared micromulsion formulation was converted into gel form using carbopol 934 (1.5%) known as aceclofenac loaded topical Emulgel. The  ex-vivo study were performed and compared with marketed available gel.

Free Coaching Class for PG-CET at Parul Institute of Pharmacy

“Parul group of Institutes” is a multidisciplinary hub of 19 self financed institutions with more than 15000 students and a thousand eminent faculty members.
We work with a vision of providing a horizon less sky of knowledge and excellence and strive hard to build a rewarding future for our students. The team of Parul Group is united by a common desire to work towards advancement of our nation & boost its economy through development of dynamic & industrious work-professionals. Our mission is to groom enlightened technocrats, leaders and generate the ideas that provide solutions to our most challenging socio-economic problems.

STUDIES IN CONCURRENT PROCESS VALIDATION OF CEFIXIME DISPERSIBLE TABLET I.P.

ABOUT AUTHORS:
Mr. Diptesh A. Patel1*, Mrs. Pinkal H. Patel1, Mr. Rohit K. Patel2
1Department of Quality Assurance, Baroda college of pharmacy, Vadodara, Gujarat, India.
2Department of Quality Assurance, Kaptab Pharmaceutical, Vadodara, Gujarat, India.
*dipteshpatel88@yahoo.com

ABSTRACT
The purpose of the research investigation was to study concurrent Process Validation of Cefixime Dispersible TabletI.P. These processes should be controlled in order that the finished product meets all quality specifications. The critical process parameters were identified with the help of process capability and evaluated by challenging its lower and upper release specifications. Three initial process validation batches of same size, method, equipment and validation criteria were taken. The critical parameter involved in sifting, sizing and compression stages were identified and evaluated as per validation plan. Uniformity of mixing is optimum in 30 min as standard deviation was between ±0.20% to ±0.99%. Compression speed of 16 RPM was suitable for IPQC as  % standard deviation limits was found for Thickness was ±1.8 % to ±3 %, Hardness ±16.6 % to ±37 %, Weight Variation ±0.3% to ±7.1 %, Friability ±2.4 to ±7.1 %, Diameter ±0.9 % to ±1.2 % and Disintegration time NMT 3 min. The outcome indicated that this process validation data provides high degree of assurance.

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Opening for M.Pharm for research project in MS University

The Maharaja Sayajirao's grandson Sir Pratapsinghrao Gaekwad who founded the Maharaja Sayajirao University and settled the trust as desired by his grandfather. This Trust known as Sir Sayajirao Diamond Jubilee and Memorial Trust exists today also and caters to the educational and other needs of the people of the former state of Baroda.

SIMULTANEOUS SPECTROPHOTOMETRIC ESTIMATION OF DICLOFENAC SODIUM AND EPERISONE HYDROCHLORIDE USING ABSORBANCE RATIO METHOD IN CAPSULE DOSAGE FORM

ABOUT AUTHORS:
Lalit F. Raiyani*1, Dharanant V. Borakhatariya2, Bhargav D. Patel3, Kuldip R. Marwada4, Dr.Priti D. Trivedi5, Mr.Rajendra K. Patel6
1Parul institute of Pharmacy, Vadodara
2B. K. Modi Government Pharmacy College, Rajkot
3Ramanbhai Patel College of Pharmacy, Changa
4R. K. College of Pharmacy, Rajkot
5Professor at K. B. Institute of Pharmaceutical Education and Research, Gandhinagar
6Lecturer at K. B. Institute of Pharmaceutical Education and Research, Gandhinagar
*lalitraiyani@gmail.com

ABSTRACT:
A simple, rapid, sensitive, precise and accurate UV-spectrophotometric method (absorbance ratio) was developed and validated for simultaneous estimation of Diclofenac sodium and Eperisone hydrochloride in pharmaceutical capsule dosage form. In absorbance ratio method absorbance measurement of sample at 239.2 nm (isoabsorbtive point, λ1) and 256 nm, λ2.The absorbance ratio method was developed using methanol as solvent. Developed method is linear between 4-12µg/ml and 5-15µg/ml for diclofenac sodium and eperisone hydrochloride respectively. The mean % recovery was found to be 99.68% & 99.14% for diclofenac sodium and eperisone hydrochloride respectively.

Opportunity to work as Assistant Director in All India Council for Technical Education

The All India Council for Technical Education (AICTE) was established by an Act of Parliament (No. 52 of 1987) with a view to provide proper planning and coordinated development of the technical education system throughout the country, the promotion of qualitative improvements of such education in relation to planned quantitative growth and the regulation and proper maintenance of norms and standards in the technical education system and for matters connected therewith.

Launch of Computer Based Online Graduate Pharmacy Aptitude Test ( GPAT ) - 2013 for admission in Post Graduate Pharmacy Programme

The Scores in Graduate Aptitude Test for Engineering (GATE) have been in use till the year 2010 for admission in Master’s Programme in Pharmacy (M.Pharm) & Engineering and also for awarding fellowships / scholarships to Pharmacy Graduates along with engineering graduates. Graduate Pharmacy Aptitude Test (GPAT) an all India Examination was then launched by All India Council for Technical Education, New Delhi separately with effect from academic year 2011 - 12 for admission in Master’s Programme in Pharmacy (M. Pharm) and for award of fellowships.

Walk in - Multiple opening for Sales Officers in Ajanta Pharma

Ajanta Pharma Limited is an emerging, global pharmaceutical company with proven capabilities in the areas of product research, manufacturing & marketing.