www.medesun.com Healthcare Solutions Hyderabad : Medical Coding, Medical Billing Training

[Admin]

Medesun Healthcare solutions is classroom and online medical coding school and online medical billing school .

Fully prepares you for advancement opportunities
· Industry Renowned Training 1. Affordable
2. Personal Student & post training Support
3. CPC/CMBS/CHA/CCAT/CPAT exam boot camps
4. 100% job oriented and Certification oriented training
5. Hundreds of practice questions and answers with rationale
6. Course Completion certificate


Medesun training program will provide the student with the knowledge and understanding to analyze medical records and assign codes to classify diagnoses and procedures while applying the principles of professional and ethical conduct.

Experienced medical coders make great money because properly coded medical reports mean more income for the doctor.

Our ultimate goal is to prepare students academically, personally and professionally for successful careers in their chosen fields.


Registered Office :
Medesun Healthcare Solutions
3-6-748, Street # 12,
Himayath Nagar,
Hyderabad,
India - 500029
Ph:+91- 040-42030431, +91-9966933693,
E-Mail: info@medesun.com

http://www.medesun.com

[allstatebilling]

Medical Billing and Coding provides error-free electronic claims processing and helps you with a steady cash flow!

[Guest]

CURRICULUM-VITAE
Name : Dr. Dinesh N. Shinde
Email : dr.dinesh_shinde AT yahoo.com
dr.dineshshinde80 AT gmail.com
OBJECTIVE :
To obtain challenging and responsible position where I can contribute to the successful growth of the organization using my skills and hard work. Skilled at learning new concepts quickly, working well under pressure and communicating ideas clearly and effectively.
EDUCATIONAL QUALIFICTION :
* PG Diploma in Clinico-Regulatory & Patents from Institute of CAHS [Center for Advance Health Science, Ramnarayan Ruia College Matunga (E), Mumbai.]
Academic Year : 2008
* Bachelor of Homeopathic Medicine and Surgery
Venutai Yashwantrao Chavan Homeopathic Medical College, Kolhapur.
Academic Year : 2004
* Participated in CPCR (Cardio Pulmonary Cerebral Resuscitation) training at KEM hospital, Mumbai.
Academic Year : 2009
* H.S.C from N.G. Acharya & D.K. Marathe College, Chembur, Mumbai.
Academic Year : 1998
* S.S.C from patwardhan high school, Govandi, Mumbai.
Academic Year : 1996
WORK EXPERIENCE :
* Total experience of 6 yrs in Health Care Industry which includes a 2.5 yrs experience in Clinical Research.
* Presently working with DMRI (Drug Monitoring research Institute) rabale, navi Mumbai & also with Mayfair Clinical Education and Research Centre, Thane (Since 2.5 yrs) as a Clinical Research Associate cum Clinical Research Physician.
* Worked as Resident Medical officer at Prakruti Hospital, Kalwa, Thane from Jan 08 to Dec 08.
* Worked as Resident Medical officer at Risk Care Hospital, Charai, Thane from Jan 07 to Dec 07.
* Participated in Bioequivalence study sponsored by Auden McKenzie Ltd. UK . (For MHRA Submission.)
* Practicing General Medical practice in own clinic since Jan 07.
WORK PROFILE :
* Adverse Event Management, Interpretation, and Reporting within timeline, SAE Reconciliation.
* ADR/AE/SAE Report Preparation, Documentation and Reporting Using CTCAE Medical Dictionaries.
* Contributing to CRF Designing and Assisting Medical Writer in Protocol Preparation, Reviewing Medical Literature, Safety Data.
* Clinical Review of All Cases - Serious and Non-Serious Safety Reports.
* Review and Verify Appropriate Selection of Adverse Events from source Documents, Appropriate CTCAE for Each Adverse Event and Accuracy of Label Assessments for Each Adverse Event.
* Contributing To Preparation of Clinical Study Reports.
* Informed Consent Presentation and Review.
* Medical care of Subjects throughout the Study.
* Review and completion of CRF's, Ensuring Accuracy of all Records keeping the number of data queries low.
* Conducting Bioequivalence Studies, Clinical Trials according to Protocol and ICH-GCP Guidelines.
SKILLS & QUAILITIES :
* Sound Knowledge of ICH-GCP, Schedule Y, ICMR, CIOMS, Clinical Pharmacology, Pharmacovigilance, FDA and EMEA regulation.
* Worked on Protocol designing, CRF designing, Informed Consent form, Subject recruitment, Study conduct, Ethical correspondence.
* Willingness to learn & work in challenging environment.
* Comprehensive and excellent direct patient care skills, problem solving and management skills.
* Good oral and written communication skills.
* Quick learner, Committed and able to work under pressure
COMPUTER EXPERTISE :
Operating System : Windows 98, Windows XP, Windows Vista.
Office Suit : Microsoft Office (Word/Excel/PowerPoint)
EXTRA-CURRICULAR ACTIVITY :
* Participated in PULSE POLIO CAMP, Thane.
* Participated in Blood Group Detection, Donation camp.
* DOT Provider at Thane Municipal Corporation.
* Participated in seminar on HIV & Related Diseases. Active participation in Inter College Cricket Tournaments.

[Guest]

CURRICULAM VITAE
S.SANTOSH KUMAR
Email id :santooosh_2004 AT yahoo.co.in

CARRIER OBJECTIVE :
‘’To work as a professional environment where I can contribute myself and enrich my analytical and technical skills according to the latest technologies and to work towards achieving the organizational goals’”
STRENGTHS :
1. Ability work in a team with high-level involvement
2. Good communication and interpersonal skills
3. Self-confidence and self motivate
Qualification Institute / University Years of study Percentage Result
M. Pharmacy
(Pharmaceutics)
Vels University
Chennai 2009-11 68
First Class
B. Pharmacy Trinity college of pharmaceutical sciences,peddapalli.
K.U 2004-08 68
First Class
Intermediate
(Bi.P.C) Krishnaveni Junior College kothagudem,Khammam DT
Board of intermediate 2000-2002 80.1 First Class with Distinction
S.S.C. RamaKrishna High School, Paloncha,Khammam DT 1999-2000 65 First Class
PROFESSIONAL QUALIFICATIONS :
AREA OF INTEREST :
- Pharmacovigilance
I have undergone training in the following Areas :
- Causality Assesment
- Expedited Reporting
- MedDRA
- Aris g
- PSUR&ICSR
- Signal Detection Tools
- Pharmacovigilance Regulatory Guidelines
- Pharmacovigilance Real Time
I have completed a certified course on CLINICAL TRIALS AND PHARMACOVIGILANCE
- Clinical Trial
- Regulatory affairs
- FR & D
- Quality Assurance
ACADEMIC PROJECT (M. Pharm.) :
PROJECT TITLE : Formulation and Evaluation of Metoclopramide Hydrochloride Buccal Tablets by Direct Compression Method at VELS UNIVERSITY, CHENNAI.
KEY SKILLS :

1. A precise knowledge on Production related QA activities and GCP,cGMPP ,GLP.
2. A precise knowledge on Drug regulatory affairs, US-FDA Drugs & Cosmetic act.
3. System (computer) knowledge : MS-OFFICE.
POSITIVE TRAITS :
- Good Communication and interpersonal skills.
- Ability to work hard for the organization and dedication to the given work.
- Able to work as a part of a team and also an individual.
- Quick Learner and Positive thinking.
DECLARATION :
I hereby declare that the information given above is genuine to the best of my knowledge and brief and if you give an opportunity to work in your organization, I will put my best efforts.
Place Best Regards
Hyderabad S.Santoshkumar

[Guest]

is there any necessity know the pure/complete english to training of coding