🧪 Pharmaceutical Reference Standards – Professional Page Content

High-Purity Standards for Accurate & Reliable Analysis

At Servona Tech , we provide high-quality certified reference materials (CRMs) essential for accurate analytical testing, quality control, and regulatory compliance in the pharmaceutical industry. Our reference standards are carefully characterized and traceable to internationally recognized sources, ensuring reliable results across your testing processes.

Whether you’re conducting method validation, impurity profiling, or routine QC analysis — our reference standards support precision and compliance every step of the way.

📄 Introduction:

Pharmaceutical reference standards play a crucial role in ensuring the accuracy and reproducibility of analytical results during drug development, manufacturing, and quality control. At Servona Tech, we supply a wide range of active pharmaceutical ingredients (APIs), impurities, degradation products, and excipients used as references in analytical procedures.

All our materials are accompanied by comprehensive documentation, including certificates of analysis (CoA), chemical specifications, and storage instructions — ensuring full traceability and compliance with pharmacopoeial and regulatory requirements.

✅ Key Features:

1. Wide Range of Standards

We offer a broad selection of reference standards for both innovator and generic drugs, including:

  • Active Pharmaceutical Ingredients (APIs)
  • Process & Degradation Impurities
  • Metabolites
  • Excipients
  • Degradation Products

2. High Purity & Traceability

All our reference standards are tested for purity, identity, and stability using advanced analytical techniques, and are traceable to international standards (USP, EP, BP, JP).

3. Comprehensive Documentation

Each reference standard is supplied with a detailed Certificate of Analysis (CoA) containing:

  • Chemical & Spectral Data
  • Purity Assessment
  • Storage Conditions
  • Expiry Date
  • Safety Information

4. Custom Requests Accepted

If you require a specific reference material not listed in our catalog, our team can assist in sourcing or synthesizing the required compound based on your project needs.

5. Regulatory Compliance

Our reference standards meet the requirements of major pharmacopoeias and regulatory bodies such as ICH, FDA, EMA, USP, and EP — making them ideal for use in GMP-compliant laboratories.

🎯 Why Choose Servona Tech?

  • Reliable Source: We ensure consistency, quality, and reliability in every batch of reference materials.
  • Scientific Expertise: Our team includes experienced chemists who understand the critical role of reference standards in analytical science.
  • Quick Turnaround: Fast processing and delivery options tailored to your research or production timelines.
  • Client Support: We provide technical assistance and documentation guidance upon request to support your regulatory submissions.

💬 Looking for Certified Reference Materials?

Let Servona Tech be your trusted supplier of high-quality pharmaceutical reference standards.
👉 Contact Us today for product inquiries or custom requests.

📍 Contact Information:

Servona Tech
📧 Email: [email protected]
📞 Phone: +201009076870
📍 Address: 393 Building, 5th District, 6th City of October, Giza, Egypt