Sentara Labs
Drug Compounding Division
Pharmaceutical &
Drug Compounding
GMP certified sterile and non sterile formulations supported by controlled manufacturing environments, validated procedures, and quality assurance oversight.
End to End Support
Compounding and
Manufacturing Support
Our drug compounding services are designed to support organizations operating in regulated environments that require reliable formulation expertise, controlled production processes, and documented quality systems.
From early stage development through production, we maintain structured operating procedures, process controls, and quality review protocols to help ensure consistent product performance and compliance readiness.
Each project is supported by technical collaboration, process planning, and quality oversight throughout the manufacturing lifecycle.
Formulation Expertise
Technical collaboration on formulation requirements from early stage development through production.
Controlled Production
Structured operating procedures and process controls maintained across all compounding activities.
Quality Oversight
Documented quality review protocols integrated throughout the manufacturing lifecycle.
Compliance Readiness
Quality systems designed to support partners operating in regulated pharmaceutical environments.
What We Compound
Compounding Capabilities
We provide flexible pharmaceutical compounding across multiple dosage forms and therapeutic applications.
Sterile Compounding
Preparation of sterile formulations within controlled production environments using validated preparation and contamination control procedures.
Non-Sterile Compounding
Manufacturing of non-sterile pharmaceutical preparations across multiple dosage formats with consistent process monitoring.
Active Pharmaceutical Ingredient Integration
Precise incorporation of APIs into custom formulations with controlled measurement, blending, and verification procedures.
Topical and Transdermal Formulations
Creams, gels, ointments, and delivery systems produced under documented formulation and mixing protocols.
Oral Liquids and Suspensions
Compounded liquid preparations designed for dosing accuracy, stability, and therapeutic consistency.
Compliance & Quality
Regulatory and Quality Framework
Our operations follow GMP certified manufacturing standards supported by structured documentation, controlled production procedures, and quality assurance review.
We maintain a quality framework aligned with regulatory expectations to support pharmaceutical and healthcare partners requiring reliable manufacturing environments.
Documented formulation and batch protocols
Controlled production environments
Process monitoring and verification
Quality assurance oversight
Testing and release controls
This structured approach supports consistency across batches while maintaining readiness for regulated projects.
Quality Assurance
Quality Assurance
and Testing
Quality verification is integrated throughout the compounding process to help ensure formulations meet required specifications and safety expectations prior to release.
Products are released only after quality review confirms that specifications and testing requirements have been met.
Request a ConsultationAnalytical Testing
Testing to verify identity and potency of active pharmaceutical ingredients against defined specifications.
Microbial and Contamination Screening
Microbial and contamination screening where applicable to formulation type and intended use.
Physical and Chemical Evaluation
Physical and chemical property evaluation performed per batch and documented throughout the process.
Batch Documentation Review
Batch documentation review and verification conducted prior to any release determination.
Quality Approval Prior to Release
All products subject to quality approval before release. No product is released without review confirmation.
Facility
Controlled Manufacturing
Environment
Compounding activities are performed within controlled manufacturing environments designed to support precision, repeatability, and contamination control.
Our facilities support the following controls across all production stages.
These controls help ensure consistent product outcomes across development and production runs.
Validated Equipment
Validated equipment and calibrated instruments maintained across all production stages.
Material Handling
Controlled material handling procedures applied from receipt through production and storage.
Environmental Monitoring
Environmental monitoring practices maintained throughout compounding operations.
Operating Procedures
Standard operating procedures governing each stage of the production process.
Our Process
Structured From
Formulation to Release
Every project follows a controlled workflow designed to support consistency and predictable outcomes.
Consultation
We align on project requirements, formulation scope, and quality expectations before work begins.
Formulation
Technical planning and formulation development guided by validated procedures and process controls.
Production
Compounding activities conducted within controlled manufacturing environments under documented operating procedures.
Testing
Quality verification performed against defined specifications prior to any release decision.
Release
Products are released only after quality review confirms that all specifications and testing requirements have been met.
Working Together
Partner Collaboration
We work closely with partners throughout development and production to align technical requirements, timelines, and quality expectations.
Our structured approach supports efficient project execution and reliable manufacturing outcomes.
Industries We Support
Who We Work With
- Pharmaceutical companies
- Biotechnology organizations
- Healthcare providers
- Clinical programs
Reliable Manufacturing
Reliable Manufacturing for Regulated Environments
Sentara combines formulation expertise with controlled manufacturing processes and quality oversight to support partners operating in regulated pharmaceutical environments.
REQUEST A QUOTE
For inquiries or assistance with your formulation needs, please do not hesitate to contact us.