Operational Governance & Regulatory Overview

Certifications, Licenses & Regulatory Compliance

Avand Kashef Tasnim (AKT) operates under full regulatory compliance with local and international bio-resource management guidelines. Our integrated supply chain—spanning bio-resource breeding, controlled venom extraction, analytical characterization, and product development—is validated by competent national and international environmental and health authorities.

By combining controlled biological management with high-throughput characterization protocols, we provide full batch-to-batch reproducibility and dynamic traceability across research-grade and preclinical applications.

Company Reg. No. 51850 Non-CITES Trade Baseline IFDA / MOHME Validated ISO/IEC 17025 Workflows

Environmental Bio-Farming Closed-loop arachnid housing & extraction licensing

Global Trade Compliance Verified non-CITES export & customs documentation

IFDA Health Manufacturing MOHME pharmaceutical oil & cosmetic licenses (2029)

Analytical QA/QC Traceability Lot-specific Certificate of Analysis (CoA) for all batches

Controlled Bio-Resource Facility & Housing Infrastructure

Industrial-scale controlled environment featuring modular arachnid housing units with continuous biometric and climatic monitoring.

Controlled Climate (IoT) Modular Housing Units ISO/IEC 17025 Compliant

Captive Colony Management & Welfare

Specialized arachnid husbandry protocols ensuring biological vitality and zero cross-contamination.

High-Welfare Standards Zero Contamination

Species Verification & Taxonomic Integrity

Rigorous morphological classification and non-CITES certification across all bio-resource batches.

Taxonomic Verification Non-CITES Certified

Permits & Trade Compliance

Official Regulatory Licenses & Authorizations

Government operating licenses, environmental committee authorizations, international CITES assessments, and health ministry establishment permits covering closed-loop arachnid management and biopharmaceutical cosmetic manufacturing.

01
Large-Scale Bio-Facility & Breeding License

Active & Valid

Operational Mandate & Biosafety Scope
Authorized operation of an industrial-scale closed-loop scorpion breeding, housing, bio-resource preservation, and venom extraction bio-facility under strict sanitary and biosafety protocols.

Up to 4,000,000 Scorpions 218,640 m² Land Footprint Closed-Loop Biosafety Sanitary Control

Issuing Authority

Fars Province Environmental Organization (DOE)

Permit & Committee Ref.

10th Committee (Ref. 15190 / Delegation 97/4904)

Approved Capacity

4,000,000 Scorpions

Facility Footprint

2,000 m² Facility (21.86 ha Land)

Status: Active & Validated by Provincial Environmental Delegation
Request Verification & Dossier
02
CITES Assessment & International Trade Compliance

CITES Non-Listed

International Regulatory Determination
Official confirmation that our managed scorpion species are not listed in CITES Appendices (I, II, or III). Consequently, CITES export permit controls do not restrict international research-use shipments.

Non-CITES Trade Status Material Transfer Standard Customs Fast-Track Global Research Supply

Regulatory Body

Ministry of Agriculture and Forestry, Turkey

Document Reference

E-62600533-283.02.01-23845921

Covered Taxa

Our Managed Bio-Species & Non-Listed Taxa

Export Governance

Standard Bio-Customs & CoA Declarations

Verified: Export clearance verified under international non-CITES protocol
Request Trade Clearance Verification
03
Biopharmaceutical & Non-Edible Oil Manufacturing Permit

Valid to 2029

Formulation & Bio-Processing Mandate
Production, processing, and formulation of hygienic and biopharmaceutical-grade non-edible oils under strict sanitary regulations within the university biotechnology incubator.

Biopharmaceutical Grade Non-Edible Bio-Oils IFDA Regulatory Baseline Pharmacy Faculty Incubator

Issuing Authority

MOHME / IFDA – Shiraz University of Medical Sciences

Permit Number

3209667941

Facility Base

Biotech Growth Center, Faculty of Pharmacy

Validity Period

Valid through February 2029

Health Ministry Registration: Verified under IFDA Technical Standard
Request Health Permit Verification
04
Cosmetics & Personal Care Manufacturing License

Valid to 2029

Cosmeceutical Production Authorization
Manufacturing of specialized cosmetic formulations, personal care lines, skin, body, and topical applications incorporating bio-functional derivatives under strict quality control.

Topical Formulations Bio-Functional Derivatives Personal Care Lines MOHME Compliance

Issuing Authority

MOHME / IFDA – Shiraz University of Medical Sciences

Permit Number

5858119558

Facility Base

Biotech Growth Center, Faculty of Pharmacy

Validity Period

Valid through August 2029

Health Ministry Registration: Fully Licensed for Bio-Cosmetic Lines
Request Cosmetic Permit Verification

Technopark & Commercialization

Ecosystem Integration & Strategic Roadmap

Operating within specialized biotechnology incubator zones, AKT connects biological resource management directly to analytical characterization, preclinical contract research, and international supply.

Research-Grade Venom Supply

Standardized, high-purity raw and fractionated scorpion venom supplied with lot-specific Certificate of Analysis (CoA) for academic institutions, CROs, and biotech laboratories worldwide.

Purity ≥ 98% Lyophilized Powder Lot-Specific CoA

Bioassay Screening & IC50 Profiling

Specialized in vitro cytotoxicity screening, cell viability testing, IC₅₀ determination, and selectivity profiling to support early-stage oncology and ion-channel drug discovery programs.

IC50 Testing Cytotoxicity Profiling Ion-Channel Targets

Full Batch Traceability

Every delivered vial is linked to a permanent batch record detailing species taxonomy, biological extraction date, freeze-drying parameters, and chromatographic purity metrics.

Unique Lot ID Chromatography Data Full Chain of Custody

Quality Standards & Partnerships

Facility base supported by ISO/IEC 17025 testing frameworks and strict biosafety discipline. Connect directly with our scientific team to discuss custom supply agreements.

Inquire for Supply & Partnerships

Analytical SOPs & Proteomic Workflows: For detailed technical documentation regarding our 4-stage analytical workflow (LC-MS/MS, RP-HPLC-PDA, MALDI-TOF, Tricine SDS-PAGE, and Raman spectroscopy), explore our dedicated Research & R&D Platform.

Clarifications & Guidance

Frequently Asked Questions

Essential regulatory, export governance, and analytical documentation guidance for academic institutions, CROs, and pharmaceutical development partners.

How does AKT fulfill international CITES and customs export compliance?

Our managed working species are officially evaluated by regulatory and agricultural authorities (Ref. E-62600533-283.02.01-23845921) and confirmed as non-CITES listed (not restricted under CITES Appendices I, II, or III). Global research shipments are accompanied by authenticated Material Transfer Declarations, Certificate of Analysis dossiers, and validated customs clearance declarations.

What analytical documentation accompanies a research-grade venom order?

Each delivery is accompanied by an authenticated Lot-Specific Certificate of Analysis (CoA). This comprehensive dossier includes high-resolution RP-HPLC chromatograms, total protein quantification (BCA/Kjeldahl), SDS-PAGE electromobility profiles, and validated reconstitution and storage guidelines.

Are custom fractionation reports available under Non-Disclosure Agreements (NDAs)?

Yes. In-depth LC-MS/MS sequence deconvolution, specialized IC₅₀ cytotoxicity curves, and tailored fractionation profiles can be provided to qualified institutional and commercial partners under standard NDAs. You can initiate a confidential technical inquiry through our contact portal.