Nadiad

Walk in for Trainee Medical Representative in Systopic Labs

Systopic Laboratories Pvt. Ltd. was incorporated in the year 1984 with an objective to provide quality innovative therapeutic solutions. The guiding principle at Systopic is pursuit of  "Excellence through People & Innovation". This dictum forms the basis of all thinking & action at Systopic.
We at Systopic strive hard to retain & build on the goodwill and trust of the medical fraternity, earned by us over a period of 27 years. The basis of which is consistently exceeding customer expectations & keeping patients interest on-top. Practitioners across varied medical specialities patronize our formulations, recognizing our status as a prominent prescription oriented company.

Post : Medical Representative - (Trainee)

Job Opening in Comed for posts of Zonal Sales Manager, Regional Sales Manager, Divisonal Sales Manager, MR

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.

FORMULATION AND EVALUATION OF DRY SYRUP CONTAINING LINEZOLID

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ABOUT AUTHORS:
Akash M Patel*, Viren N Sisodiya
* Faculty of Pharmacy,
Dharmsinh Desai University, Nadiad-387001, Gujarat
aku.pharmacy@gmail.com

ABSTRACT
Taste is an important factor in the development of dosage form. The problem of bitter and obnoxious taste of drug in pediatric patient can create a bad psychological effect on mind. The purpose of this research was to mask the intensely bitter taste of Linezolid using ion exchange resin and to formulate the dry syrup of the taste masked drug. When suspension is swallowed the bitter taste of the drug may not be felt as ion exchange resin does not release the drug at salivary pH. When it comes in contact with acidic environment of stomach, the complex will be broken down releasing the drug which may then absorbed. Batch method was used for formation of drug resin complex. Various ion exchange resin like different grade of kyron and indion 214 were used for masking the bitter taste. Optimization of drug loading was carried out. Indion 214 was selected as a optimized resin with 84.47 % drug loading. Dry syrup was made using suspending agent like gellan gum, guar gum and CMC and evaluated for various parameters like colour, odour, taste, viscosity, sedimentation volume, redispersibility, % drug content, drug release. By evaluating all the parameter the batch formulation contained guar gum 3 % was the best one amongst all the other formulations.

Vacancies for Pharmacists in Gujarat State AIDS Control Society

Gujarat state is one of the highly industrially developed states in the country. Being an industrialized state, migration of laborers from various parts of India is very high. Mobility and migration of people make them more vulnerable, as a result of separation from spouse and release of social sanctions, leading to high-risk sexual practices and consequently they may contract HIV, which in turn is carried to their spouses and to their children.

ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR SIMULTANEOUS ESTIMATION OF TOLPERISONE HYDROCHLORIDE AND DICLOFENAC SODIUM IN BULK AND PHARMACEUTICAL FORMULATION

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ABOUT AUTHORS:
Akash M Patel*, Nirav N Patel, Prakash A Sathwara
*Faculty of Pharmacy, Dharmsinh Desai University,
Nadiad, Gujarat
Aku.pharmacy@gmail.com

ABSTRACT
Quantitative analysis of any drug is an important tool in an industry. It is important to determine that the raw material, intermediate products as well as final products meet its specifications and are of required quality. The number of drugs and drug formulations introduced into the market has been increasing at an alarming rate. These drugs or formulations may be either new entities or partial structural modification of the existing ones or novel dosage forms.

Spectrophotometry and HPLC methods are considered to be most suitable for estimation of the drugs present in pharmaceutical dosage forms.

· Literature review reveals that several spectroscopic and Chromatographic method have been reported for estimation of TOL and DIC alone as well as with other drugs.
· Simultaneous equation, dual wavelength difference UV spectrophotometry and First derivative spectroscopic method is available for this combination.
· The aim of work is to develop and validate cost effective First derivative method in water and RP-HPLC method for simultaneous estimation of TOL and DIC in bulk and Tablet dosage form.
· Development of UV spectrophotometric method.

Recruitment of JRF in DST-Fast Track project at Shah- Schulman Center for Surface Science and Nanotechnology, Dharmsinh Desai University

It was in 1968 that Late Shri Dharmsinh Dadubhai Desai founded Dharmsinh Desai Institute of Technology with one Department of Chemical Engineering offering an UnderGraduate course and a Diploma course in Chemical Engineering. The objective was to provide technical education and prepare students for the needs of the industry. Various engineering departments were successively added.

Application on plain paper are invited from eligible candidates with detailed biodata supported by duly attested copies of certificates for the following research position in DST supported Fast-Track research project. Short listed applicants will be invited before a selection committee for interview at Dharmsinh Desai University. No TA/DA is admissible for attending the interview.

A VALIDATED STABILITY- INDICATING HIGH PERFORMANCE LIQUID CHROMATOGRAPHIC METHOD FOR DARUNAVIR ETHANOLATE IN TABLET DOSAGE FORM

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ABOUT AUTHORS:
Palak G. Chaudhary1*, Bhavini N. Patel1, Chhagan N. Patel2
1Department of Quality Assurance,
2Department of Pharmaceutical Chemistry
Shri Sarvajanik Pharmacy College, Mehsana, Gujarat, India.
*palakc24@gmail.com

ABSTRACT
High performance liquid chromatographic method was developed and validated for the determination of Darunavir Ethanolate in tablet dosage form. The method was carried out on a Phenomenex luna C18 Column (150 × 4.6 mm id, 5µ) maintained at 30oC. The mobile phase consisted of water-acetonitrile (60 + 40, v/v) pumped at a flow rate 1.0 mL/min. Photo diode array detection was at 265 nm. The chromatographic separation was obtained with a retention time of 11.8 min, and the method was linear in the range of 1-30 µg/mL (r2 = 0.9997). The specificity and stability indicating capability of the method was proven through forced degradation studies, which also showed that there was no interference of the excipients. The method was validated for linearity, precision, accuracy, robustness, specificity, limit of detection and limit of quantitation. The developed method, after being validated was successively applied to the analysis of tablet formulations. The drug could be effectively separated from different degradation products and hence the method can be used for stability analysis.

Job for Professional Service Representatives (26 Posts) in KAPL - Government Enterprise

Karnataka Antibiotics & Pharmaceuticals Ltd., (KAPL) Bangalore is a Government Enterprise.  From a modest beginning in 1984, KAPL has grown from strength to strength in the areas of manufacturing and marketing of various life saving and essential drugs. With an ISO accredition from KPMG, Netherlands, KAPL is recognised for its total commitment to quality and services in domestic and international markets. On profit from inception, KAPL facilities are approved by many international clients.

Post: PROFESSIONAL SERVICE REPRESENTATIVES [PSRs]

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