Clinformatiq

Start your career with Clinformatiq’s job-oriented training program.

Gain practical training and industry-focused skills in Clinical Research, Clinical Data Management, and Pharmacovigilance, with career support.

Open to B.Pharm, M.Pharm, Pharm.D, and Life Science graduates.

New batch starting soon.
Limited seats available.

Call Now: +91 9010855577
Website: clinformatiq.com
Email: [email protected]

Start your career in the healthcare industry with the Medical Coding Training Program at Clinformatiq.

Get industry-oriented training in Medical Terminology, Anatomy, Physiology, Pharmacology, ICD-10-CM, CPT, HCPCS, E&M Coding, inpatient and outpatient coding, compliance guidelines, and medical records documentation.

The program includes practical exercises, real-time case studies, interview preparation, career guidance, and placement assistance.

Course Duration: 6–8 Weeks
Mode: Live Online / Classroom
Batches: Weekday and Weekend

Eligible qualifications: B.Pharm, Pharm.D, M.Pharm, B.Sc/M.Sc Life Sciences, Nursing and Biotechnology graduates.

Enroll now and build your career in Medical Coding.

Website: clinformatiq.com
Call: +91 9010855577
Email: [email protected]

Congratulations Navya for placing in Laila Nutraceuticals👏🎉

The future of healthcare runs on accurate data, and Clinical Data Management is at the heart of every successful clinical trial.

At Clinformatiq, our Clinical Data Management (CDM) program is designed to help aspiring professionals build industry-ready skills through practical learning. Gain hands-on experience with live EDC tools, understand CRF design, learn CDISC standards, master query management, and work on real-time clinical trial workflows under experienced industry trainers.

Whether you're a Life Sciences graduate, Pharm.D, B.Pharmacy, M.Pharmacy, B.Sc, M.Sc, Nursing, or looking to build a career in Clinical Research, this program provides the practical exposure employers value.

Join Clinformatiq and take the first step toward a career in Clinical Data Management.

For admissions:
Website: www.clinformatiq.com
Call: +91 9010855577
Email: [email protected]

Build a successful career in Regulatory Affairs with industry-focused training designed to make you job-ready.

Clinformatiq offers practical learning through real-time regulatory projects, CTD and submission training, mock interviews, resume preparation, and placement support. Learn from experienced industry professionals and gain the skills required to enter the pharmaceutical and life sciences sectors with confidence.

Key Highlights:
• Industry Expert Trainers
• Real-Time Regulatory Projects
• Hands-on CTD & Submission Training
• Mock Interviews and Q&A Sessions
• Resume Building Support
• Interview Preparation
• Placement Assistance

Limited Batch | High Demand Course

Enroll today and take the next step toward your Regulatory Affairs career

Top MNCs are actively hiring skilled Regulatory Affairs freshers, and the right training can help you stand out in the competitive pharma industry. Clinformatiq’s industry-focused Regulatory Affairs training is designed to help students and fresh graduates gain practical knowledge that companies look for during hiring.

Learn industry-relevant concepts, understand real-time regulatory processes, and improve your chances of getting selected by leading healthcare and clinical research organizations.

Companies hiring skilled RA candidates include:
• IQVIA
• Syneos Health
• Parexel
• Cognizant
• Accenture

Get trained with practical exposure and build a strong foundation for your career in Regulatory Affairs and Clinical Research.

Contact: +91 9010855577
Website: clinformatiq.com

Affairs Jobs Jobs Research

Build the skills the pharmaceutical industry is actively hiring for with Clinformatiq’s Job-Oriented Regulatory Affairs Training Program. Designed for Pharm.D, B.Pharm, M.Pharm, and Life Science graduates, this program focuses on practical industry knowledge that helps you become job-ready from day one.

Learn:
• CTD & eCTD Submissions
• ICH Guidelines
• IND, NDA & ANDA Filing Process
• Hands-on Dossier Preparation
• USFDA & EMA Regulations

This is not just theoretical learning. The training is focused on practical applications, real-time industry concepts, and career-focused guidance to help freshers enter the pharma and clinical research industry with confidence.

Contact: +91 9010855577
Website: clinformatiq.com

Build a strong career in Regulatory Affairs with Clinformatiq.

Regulatory Affairs plays a key role in the pharma industry by supporting drug approvals, product launches, and global compliance. This field offers excellent career growth opportunities for pharmacy and life sciences graduates.

Who can apply:
B.Pharm / M.Pharm / Life Sciences graduates

Why choose Regulatory Affairs?
• Opportunity to work with leading pharma companies
• Growing demand in India and international markets
• Career opportunities in drug development and approvals
• Industry-focused training and career support

Become industry ready with practical learning and professional guidance from Clinformatiq.

Contact:
+91 9010855577
[email protected]
clinformatiq.com

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