JANOSHIK VERIFIED

Pharmaceutical Excellence. Verified Quality.

Third-Party Verified Testing

At REVION+, we set the gold standard for quality assurance in pharmaceutical-grade compounds. Every batch undergoes rigorous Janoshik third-party testing to guarantee absolute purity, precise potency, and uncompromising consistency.


Our commitment to transparency means every customer receives detailed Certificates of Analysis (COA) for their products. Each certificate is independently verified, traceable, and accessible through our secure QR verification system, ensuring complete confidence in the authenticity and quality of REVION+ products.

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Pharmaceutical-Grade Standards

Manufactured in compliance with the highest international quality benchmarks, ensuring consistent potency and purity in every batch.

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Independent Verification

Every product tested by Janoshik Analytical Laboratory, the industry's most trusted third-party testing facility for identity, strength, and composition.

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Complete Transparency

End users can access detailed test results instantly through our QR verification system. Each product displays comprehensive COAs showing exact purity percentages and compound analysis.

Latest Janoshik Test Certificates

Independent third-party verification for every batch. Click to view full analytical reports

Batch Verified

REVION+ TZ 30mg

Product
Tirzepatide 30mg
Concentration
10.79 mg/ml
Purity
99.685%
Test Date
17/10/2025
Batch Verified

REVION+ TZ 60mg

Product
Tirzepatide 60mg
Concentration
20.15 mg/ml
Purity
99.712%
Test Date
17/10/2025
Batch Verified

REVION+ TZ 90mg

Product
Tirzepatide 90mg
Concentration
30.22 mg/ml
Purity
99.698%
Test Date
17/10/2025
Batch Verified

REVION+ RT 40mg

Product
Retatrutide 40mg
Concentration
10.0 mg/ml
Purity
99.5%+
Test Date
January 2026
Batch Verified

REVION+ NAD+

Product
NAD+
Concentration
1165.62 mg/ml
Analysis
Quantitative
Test Date
17/10/2025
Quality Guaranteed

Our unwavering commitment to quality extends beyond testing. From raw material sourcing to final product delivery, every step in our manufacturing process adheres to strict pharmaceutical protocols. Each batch undergoes multiple quality control checkpoints before independent third-party verification, ensuring products that meet the highest standards of purity and potency.

Transparency for your customers. Wholesalers and retailers can confidently share these test results with end users. Simply direct customers to scan the QR code on their product or enter the batch number to instantly access the complete Certificate of Analysis. Every test is independently verified and fully traceable.

Our Rigorous Testing Protocol

01

Raw Material Analysis

Every incoming raw material undergoes preliminary testing for identity and purity before entering our pharmaceutical-grade facility.

02

In-Process Control

Multiple checkpoints during synthesis ensure consistency and quality at every stage of production.

03

Final Batch Testing

Completed batches undergo comprehensive internal analysis for potency, purity, and sterility compliance.

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Janoshik Verification

Independent third-party analysis by Janoshik Laboratory provides unbiased confirmation of quality specifications.

Industry-Leading Standards

REVION+ maintains compliance with international pharmaceutical standards, ensuring every product meets or exceeds regulatory requirements for quality and purity.

USP/EP Grade Standards
ISO 17025 Certified Testing
HPLC/MS Analytical Methods
Batch-to-Batch Consistency
99.6%+
Average Purity

Across all tested batches