Advanced Regulatory Writing Course in Lucknow

Advanced Regulatory Writing Course in Lucknow

Henry Harvin® Ranks in Top 30 most Trusted Companies by Insight Success

  • ★ ★ ★ ★ ★ 4.8/5 Ratings
  • 1.1 Million Learners
  • 1455 Learner’s Rating
  • 81% Report Career Benefits

Advanced Regulatory Writing by Henry Harvin® offers exclusive sessions on clinical trial documentation, clinical study protocol, and many more | Learn about the importance of clinical trial documentation and the Role of regulatory agencies in reviewing | Be in the marketplace to grab high-paying job opportunities

Starts In 7 day

18 Nov 2024

Learning Period

96 Hours

Book a Live Class, For Free!

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Placed Learners

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Accreditations & Affiliations

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There's a reason that 95% of our alumni undertake 3+ courses as a minimum with Henry Harvin®

Know the complete offerings of our Advanced Regulatory Writing Course in Lucknow

Key Highlights

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96 Hours of Instructor-Led Sessions
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32 Hours of Live Interactive Doubt Solving Sessions
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16 Hours of Live Master Sessions by Industry Experts
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192 Hours of Self-Paced Learning
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Job-Ready Portfolio of 10 Capstone Projects
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24 Auto-Graded Assessments
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20+ Industry Case Studies
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144 Guided Hands-On Exercises
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10+ Assignments and Mini Projects
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2 Mock Interviews and 2 Hackathons
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Get 1-Year Gold Membership of Henry Harvin® School of Writing Academy
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Get a guaranteed Internship with Henry Harvin® and in top MNCs like J.P. Morgan, Accenture & many more via Forage
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Get 3 in 1 Placement support through Placement Drives, Premium access to Job portal & Personalized Job Consulting
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6 Hours of Mentorship by Industry Experts
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Earn Certification of Course from Henry Harvin®, Govt of India recognized & Award-Winning Institute and NSDC Certification

Our Placement Stats

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Average salary hike

2100+

Access the best jobs in industry

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Maximum salary hike

Access the best jobs in the industry

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You Get 10-In-1 Program

Two-way Live Training Course

Two-way Live Online Interactive Classroom Sessions

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Certification

Distinguish your profile with global credentials and showcase expertise with our Hallmark Completion certificate

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Projects

Facility to undergo various projects along with the course.

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Guaranteed Internship

Get a guaranteed Internship with Henry Harvin® and in top MNCs like J.P. Morgan, Accenture & many more via Forage.

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Placement

Get 3 in 1 Placement support through Placement Drives, Premium access to Job portal & Personalized Job Consulting

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Student Engagement & Events

Free Access to #AskHenry Hackathons and Competitions & many other facilities from Henry Harvin®

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Masterclass

Access to 52+ Masterclass Sessions for essential soft skill development

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Membership

Get Free Gold Membership of Henry Harvin®

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E-Learning Access

Free access to the E-learning Portal and future updates. Get access to PPTs, Projects, Quizzes, self-paced Video-based learning, a question bank, a library, practice tests, final assessment, a forum, and doubt sessions.

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Entrepreneurship Mentorship

Mentorship from Young Successful Entrepreneurs to set up a sustainable & scalable Business from scratch at both Freelance and entrepreneur levels

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About the Advanced Regulatory Writing Course in Lucknow

Advanced Regulatory Writing Course

The advanced regulatory writing course offers lessons on designing a clinical protocol, the Purpose and key components of the protocol, Creating an Informed Consent Form (ICF), and many more. 

10 in 1 Course

  • Training: 96 Hours of Two-Way Live Online Interactive Sessions
  • Projects: Facility to undergo projects in Creating an Informed Consent Form (ICF) and more 
  • Internship: Get Internship Support to gain experiential learning
  • Certification: Get course completion Certification of Advanced Regulatory Writing Henry Harvin® Govt of India recognized and award-winning Institute, and showcase expertise
  • Placement: 100% Placement Support for 1 Year post successful completion of the course
  • E-Learning: Free access to E-learning Portal and future updates
  • Masterclass: Access to 52+ Masterclass Sessions for essential soft skill development
  • Hackathons: Free Access to #AskHenry Hackathons and Competitions
  • Membership: 1-Year Gold Membership of Henry Harvin® Writing Academy
  • Entrepreneurship Mentorship: Mentorship from Young Successful Entrepreneurs to set up a sustainable & scalable Business from scratch at both Freelance and entrepreneur level

Trainers at Henry Harvin®

  • Most respected industry experts with 15+ years of working experience and recognized by numerous organizations over the years for their work.
  • They have delivered 400+ keynote classes for the Advanced Regulatory Writing Course
  • Have delivered 450+ lectures and are currently empaneled as domain experts with Henry Harvin® Writing Academy

Alumni Status

Become a part of the Elite Writing Academy of Henry Harvin® and join the 4,60,000+ large Alumni Network Worldwide.

Gold Membership Benefits

  • Avail 1-Year Gold Membership of Henry Harvin® Writing Academy that includes E-Learning Access through recorded Videos, Games, Projects, CPDSPe Studies
  • Access to Masterclass Sessions
  • Earn the Prestigious Henry Harvin®️ Alumni Status and become one of the reputed 4,60,000+ Alumni globally
  • Guaranteed Internship with Henry Harvin®️ or partner firms
  • Weekly 10+ job opportunities offered.
  • Experience Industry Projects during the training

Learning Benefits

  • Purpose and key components of the ICF.
  • Learn best practices for writing an ICF, including procedures, risks, and benefits.
  • Learn about writing a Clinical Study Report (CSR)
  • Work on common issues and challenges in CSR development
  • Preparing Regulatory Submissions
  • Work on the best practices for preparing regulatory submissions, including adherence to regulatory guidelines.

Know the complete offerings of our Advanced Regulatory Writing Course in Lucknow

Curriculum For Advanced Regulatory Writing Course in Lucknow

  • icons-carri22 Module 1: Introduction to Clinical Trial Documentation

    In this module, a professional will learn about Clinical trial documentation
    • Importance of clinical trial documentation in ensuring regulatory compliance and patient safety.
    • Overview of the types of documentation required for clinical trials.
    • Role of regulatory agencies in reviewing and approving clinical trial documents.
  • icons-carri22 Module 2: Designing a Clinical Study Protocol

    In this module, a professional will learn about Clinical study protocol
    • Purpose and key components of the protocol.
    • Best practices for designing a protocol, including study objectives and methods.
    • Common issues and challenges in protocol development.
  • icons-carri22 Module 3: Developing an Investigator Brochure

    In this module, a professional will learn about developing an investigator brochure
    • Purpose and key components of the brochure.
    • Best practices for writing an investigator brochure, including drug pharmacology, pharmacokinetics, and safety data.
    • Common issues and challenges in investigator brochure development.
  • icons-carri22 Module 4: Creating an Informed Consent Form (ICF)

    In this module, a professional will learn about creating an informed consent form (ICF)
    • Purpose and key components of the ICF.
    • Best practices for writing an ICF, including procedures, risks, and benefits.
    • Common issues and challenges in ICF development.
  • icons-carri22 Module 5: Writing a Clinical Study Report (CSR)

    In this module, a professional will learn about Writing a Clinical Study Report (CSR)
    • Purpose and key components of the CSR.
    • Best practices for writing a CSR, including data on safety and efficacy.
    • Common issues and challenges in CSR development
  • icons-carri22 Module 6: Preparing Regulatory Submissions

    In this module, a professional will learn about common issues and challenges in regulatory submission preparation
    • Purpose and key components of regulatory submissions, including the New Drug Application (NDA) or Biologics License Application (BLA).
    • Best practices for preparing regulatory submissions, including adherence to regulatory guidelines.
    • Common issues and challenges in regulatory submission preparation.
  • icons-carri22 Module 7: Developing a Patient Information Leaflet (PIL)

    In this module, a professional will learn about the purpose and key components of the PIL
    • Purpose and key components of the PIL.
    • Best practices for writing a PIL, including drug information, dosage, and potential side effects.
    • Common issues and challenges in PIL development.
  • icons-carri22 Module 8: Complimentary Module 1: Soft Skills Development

    • Business Communication
    • Preparation for the Interview
    • Presentation Skills
  • icons-carri22 Module 9: Complimentary Module2: Resume Writing

    • Resume Writing

Know the complete offerings of our Advanced Regulatory Writing Course

Admission Closes On 18 Nov 2024

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Upcoming Cohorts

Skills Covered

Investigator Brochure

Informed Consent Form (ICF)

Clinical Documentation

Clinical Study Protocol

Clinical Study Report

Biologics License Application (BLA)

Certifications

Get Ahead with Henry Harvin® Advanced Regulatory Writing Course in Lucknow Certification

What you'll Learn in this course

Earn your Certification

Our course is exhaustive and this Certification is proof that you have taken a giant leap in mastering the domain

Differentiate yourself with Henry Harvin®

The practical knowledge and actionable skillset you've gained working on projects, simulations, and case studies will set you ahead of the competition

Share Your Achievement

Talk about it on LinkedIn, WhatsApp, Instagram, Facebook, and Twitter, boost your resume, or frame it - tell your friends and colleagues about it.

Training Certification

Get an Advanced Regulatory Writing Course Completion Certification from Henry Harvin®

Our courses and Course Certificates are trusted by these industry leaders

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Know more about the value of this certificate in the industry

Career Services By Henry Harvin®

Career Services
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Placement Drives

We are dedicated to supporting our students throughout their career journey. Join us, and let's embark on a journey towards a successful and fulfilling career together.

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Premium access to Henry Harvin® Job portal

Exclusive access to our dedicated job portal and apply for jobs. More than 2100+ hiring partners’ including top start–ups and product companies hiring our learners. Mentored support on job search and relevant jobs for your career growth.

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Personalized Job Consulting

Share what kind of job you are looking for and we will provide you with verified job openings that match your requirement.

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Who We Are?

Henry Harvin®️ ranks amongst the Top 500 Global Edtech Companies with 4,60,000+ Alumni, 900+ B2B Clients, 500+ Award Winning Trainers, and 1200+ Courses.

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Trained

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Reviews with 4.5/5
rating

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Live Classes Every
Month

210+

Corporate Partners

180+

College Partners

87%

Reported Career
Benefits

Why Henry Harvin for the best Advanced Regulatory Writing Course

Certified & Experienced Instructors

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Gold Membership & Post Training Followups

Tailor Made Training

Flexible Schedule

Access to the Recorded Sessions

10 in 1 Program

Masterclasses By Henry Harvin®️

One-to-One Training

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