Services

At Neudrug, we deliver high-quality, compliant, and timely solutions tailored for the pharmaceutical, biotech, CRO, and healthcare IT sectors. Our core services are designed to support the entire clinical development lifecycle while ensuring regulatory and scientific excellence.

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Medical Writing

We offer comprehensive medical writing services that meet global regulatory standards. Our scientific writers combine therapeutic expertise with regulatory insight to deliver clear, concise, and compliant documents.

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Translation Services (Medical & Regulatory)

We specialize in medical translation services with a focus on accuracy, cultural relevance, and regulatory compliance. Each translation goes through a rigorous process involving certified linguists, QA reviewers, and back-translation when required.

healthcare experts team reviews x ray results to find best treatment plan

ICH GCP Training & Development

We provide high-quality, customized Good Clinical Practice (GCP) and clinical research training for clinical site teams, sponsors, and investigators to ensure compliance with ICH, FDA, EMA, and WHO guidelines.

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Medical Writing

Our offerings include:
Clinical Study Protocols & Amendments
Investigator’s Brochures (IBs)
Informed Consent Forms (ICFs)
Clinical Study Reports (CSRs)
Manuscripts, Abstracts, and Posters
Regulatory Submission Documents (IND, NDA, CTD modules)
Literature Reviews & Risk Management Plans
Plain Language Summaries

Translation Services (Medical & Regulatory)

We specialize in medical translation services with a focus on accuracy, cultural relevance, and regulatory compliance. Each translation goes through a rigorous process involving certified linguists, QA reviewers, and back-translation when required.
Specializations:
Clinical Trial Documents (ICFs, Protocols, CRFs)
Regulatory Submissions and Correspondence
Patient-Reported Outcomes (PROs) and Questionnaires
Pharmacovigilance Reports
Product Information Leaflets & Labels
Training Materials and SOPs
Certified Back Translation and Linguistic Validation

Functional Service Provider (FSP) Model

We provide scalable, dedicated, and flexible FSP support across multiple clinical and regulatory functions, ensuring cost-efficiency and quality for pharmaceutical, biotech, CRO, and digital health clients.
Our FSP expertise covers:
Clinical Trial Assistants (CTAs)
Regulatory Affairs Specialists
Data Entry & Document Management
Clinical Research Associates (CRAs)
Medical Writers and Translators
QA and Compliance Officers
Pharmacovigilance & Safety Reporting Personnel
Remote/On-site Resource Allocation

ICH GCP Training & Development

We provide high-quality, customized Good Clinical Practice (GCP) and clinical research training for clinical site teams, sponsors, and investigators to ensure compliance with ICH, FDA, EMA, and WHO guidelines.
Training Programs Include:
ICH GCP Certification for Clinical Research Staff
Clinical Trial Conduct & Ethics
Pharmacovigilance & AE/SAE Reporting
Informed Consent Process
Clinical Site Readiness and Audit Preparation
Sponsor & CRO-specific Protocol Training
Refresher and Role-Based Training Modules
Training Delivered On-site, Virtually, or On-demand

What Sets Us Apart

Experienced team of certified professionals
Fast turnaround times (e.g., RFI response within 24 hours)
Global regulatory expertise (FDA, EMA, WHO, ICH-GCP)
Quality-focused processes (SOP-driven, QC/QA layers)
Multilingual and multicultural capabilities
Flexible delivery models (FSP, full-service, ad-hoc)

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Address

Lahore, Pakistan

Email Us

info@neu-drug.com