Health Outcomes & Pharmacoeconomics Consultancy

Bridging knowledge gaps. Maximizing data potential. Advancing healthcare solutions

Founded in 2022, ECOCALL Analytics is a small boutique HEOR organization that prides itself on providing Health Outcomes & Pharmacoeconomics services.

We meet all of your HEOR needs from regulatory affairs, pharmacovigilance, development of evidence generation plans, design and execution of HEOR studies to generate needed evidence to translation of new evidence into market access intelligence and materials.

Advice & Guides

Our ambition is to bridge the gap between sound scientific data and market access.

Great Solutions

We offer services in various topcis in the regulatory affairs, pharmacovigilance, health research, and market access

Years Of Practical Experience

Guidence From Our Network of Experts

From initiation strategy to maintenance – we advise, accompany, support, and train professionals in all key areas of drug delivery.

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Success Partners

About Us

We offer advanced solutions in the following areas:

Regulatory Affairs – Pharmacovigilance – Health Research – Market Access

Over 15 years of diversified experience – Flexible agenda – Highly qualified connections and consultants

Build Stroger Pharmaceutical Industry for Public Health

Hany H Khalil

Pharmaceutical Consultant & Researcher

CEO & Founder ECOCALL U.S.

Our Vision & Mission

We take pride in putting public health front and center; committed to understanding patient needs and how we can utilize our capabilities in helping regulators, industry partners and academia excel in availability in medication management

Awards & Recognition

Years of working in mulinational organizations in advanced biopharmaceutical industries and ready to help regulators, industry partners and academia to develop and grow

Our Services

What Service We Offer

Looking for success partner?

Regulatory Strategy Development

- Designing strategic plans to facilitate regulatory compliance and market access.
- Conducting gap assessments to identify areas of improvement in regulatory processes.
- Providing guidance on regulatory requirements and standards.

Regulatory Submissions

- Preparing and submitting dossiers for new drug applications (NDAs), abbreviated new drug applications (ANDAs), and marketing authorization applications (MAAs).
- Managing electronic submissions, including electronic common technical document (eCTD) compilation and submission.

Research in Drug Safety and Quality

research services that contribute to the development, assessment, and improvement of drug safety and quality standards

Labeling and Packaging

- Reviewing and optimizing labeling and packaging materials to meet regulatory guidelines.
- Providing guidance on labeling requirements, including labeling content and format.

Pharmacovigilance

- Developing pharmacovigilance systems and processes for adverse event reporting.
- Conducting safety assessments and risk management plans.

Supply Chain Compliance

offers supply chain compliance assessments, helping companies identify gaps and implement robust processes to ensure compliance at each stage. We provide guidance on Good Distribution Practices (GDP) and help establish effective quality management systems.

We Are Open For Opportunities!

Understanding where these opportunities lie and how to access them can be extremely challenging. Our consulting and training experts guide to these opportunities with smooth market entry strategies.

Why Choose Us

We Keep You Well-updated With Latest Regulations & Technologies

Global Scientific office lisencing
Pharmacovigilance
Common Technical Dossiers
Regulatory intelligence/survey
Post-approval & life cycle management
Standard Operating Procedures (SOP)
Due diligence
Software selection & validation
Technical file constructions & review
Product classification
Packaging & labelling
Serialization and Tracability

Pharmacovigilance Studies

Studies to monitor and evaluate the safety and effectiveness of drugs on the market. Our team analyzes adverse event data, conducts risk assessments, and develops strategies to enhance patient safety.

Comparative Effectiveness Research

By analyzing real-world data and clinical evidence, we help healthcare providers and regulatory agencies make informed decisions about the most effective and safe treatment approaches.

Our Support

Let’s See Our Contributions

Our research in drug safety and quality serves as the foundation for our consulting and training services

Needs Experience Global Regulatory Affairs Consultant?

Our experts provide you with the required consultation and training to help you make smarter choices as you execute your drug development plans and researches.

We Help You to Grow Your Organisation Exponencially

We help you grow your knowledge and avoid the risk of costly mistakes.

Talk To An Expert