SUBMISSION-READY DOCUMENTS

Accelerate Your Study Start Up

Expertise, Encapsulated. We provide regulatory-compliant, culturally precise language services, including translation and medical writing, for your study teams and participants.

Trusted by Leading CROs and Sponsors

THE SAFE CHOICE FOR

Clinical Language Services

A seamless extension of your team. Our workflow is fully integrated with yours. Translation and medical writing combined.

For Participants

Comprehensible language that won't hinder your recruitment goals.

  • Informed Consent Forms (ICFs)
  • Recruitment Materials
  • Participant Materials

For Sites

Consistent communication throughout the whole clinical study lifecycle.

  • Protocols
  • Investigator's Brochures
  • Training Materials

For Internal Teams

Helping you fulfill your regulatory obligations.

  • Pharmacovigilance
  • SUSARs/DSURs
  • HA/EC Correspondence

We Are Not Generalists

We Are Specialists

Pharmaling handles exclusively clinical content. Everyone involved in your projects knows the ins and outs of clinical research.
Think of us like your language unit, outsourced.

GCP Certified Experts

Academically and professionally qualified specialists handle your documents. We act with the responsibility of a 'service provider' as defined in the newest GCP guidelines.

Aligned with Local Needs

Our workflow is organized around the local and international regulatory requirements.

Safe and Secure

Keeping your data secure and your participants safe. We only work with our trusted partners. We do not have thousands of vendors randomly assigned to your projects.

Get Smooth Approvals and Reduce Your Internal Teams' Workload

Email us at merhaba@pharmaling.com to discuss your needs.

Partner with the boutique agency that speaks the language of regulatory compliance and clinical science.