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Contract Laboratory has received the following pharmaceuticals and biopharmaceuticals Laboratory Requests which need to be fulfilled! These pharmaceuticals and biopharmaceuticals Laboratory Requests are received from a variety of sources ranging from start-up companies to large, multinational Fortune 500 corporations, international organizations, well-respected universities and government agencies that are actively seeking Labs to perform their pharmaceuticals and biopharmaceuticals Laboratory and Scientific Research. If you need a pharmaceuticals and biopharmaceuticals Laboratory, please Submit a pharmaceuticals and biopharmaceuticals Laboratory Request. If you need assistance or have questions contact us online or call toll free 1-855-377-6821. Please log in to see more.
Pharmaceutical Transportation Simulation Validation
Heparin Potency Testing
USP Inulin Monograph Testing
ICH Pharmaceutical Method Development and Validation
Skin Compound EPA 6-Pack Toxicity Testing
USP Human Albumin Protein Analysis
Pharmaceutical PVC Film Packaging Testing
NMN (Nicotinamide Mononucleotide)
Pharmaceutical Reagent Validation Testing
Biosimiliar Testing
Dermatology CDMO
Pharmacceutical LAL (Endotoxin) Testing
Triclosan Full USP Testing
Pharmaceutical Purity Assessment
Transdermal Patch ISO Biological Evaluation
Building Materials ASTM Testing
PE Sterile Bag ISO Permeability Testing
Pharmaceutical USP Raw Material Testing
P. Acnes Colonization Study
Pharmaceutical Packaging Microbial Barrier Testing
Mouthwash Bactericidal Properties
Sterile Pharmaceutical Radiochemical Purity
FDA cGMP Pharmaceutical Aerosol Propellant Testing
Somatropin Amino Acid Purity Analysis
Pharmaceutical Drug Substance Testing
Pharmaceutical Extractable Studies
6 Raw Material Certificate of Analysis | Stability Testing
FDA cGMP Pharmaceutical Analytical Laboratory
USP Packaging Testing of Elastomeric Closure for Injection
Hair Growth New Drug Development
Preclinical Inhalation Medicine Development Studies
Biological Products FDA GMP Analysis
New Drug Candidate Evaluation
Pharmaceutical USP Urea Testing
USP atomic absorption spectrometry (AAS) analysis
ASTM Surgical Sealant Burst Strength
Topical Ointment COA Certificate of Analysis
OTC Therapeutic Mouthwash Formulation
3 OTC Topical Ointments Formulation and Manufacturer
Pharmaceutical Opthalmic Solution Particulate Matter
ASTM PVC Film Biodegradation
ANSI/AAMI ECG Gel Electrical Performance Testing
Potential Illegal Drug Substance Testing
Polidocanol Potency Testing
Cleaning Validation of Levothyroxine and Liothyronine
USP Sennosides Tablets Testing
FDA GLP OECD Skin Sensitization Testing
Pharmaceutical Drug Impurity Testing
Pharmaceutical Drug Intermediate ISP-MS Analysis
Peptide Aliquot QA
Blood and Plasma Antimicrobial Drug Concentration
USP Monograph Poloxamer Testing
Collagen Aminio Acid Analysis
NIH Amino Acid Anaysis
Pharmaceutical PSD Particle Size Distribution
Pharmaceutical Bioavailability Study
ASTM API Active Pharmaceutical Ingredient Testing
USP Zinc Oxide Testing
Zioconia Beads Testing
Pharmaceutical Pharmacokinetic Ointment Reformulation and Stability
Drug Contamination Testing
Vial Seal Force Testing
Hair Inhibitor Serum Deformulation
Whole Blood Cell Surface Marker Testing
Pharmaceutical Drug Compound Analysis
Water for Injection WFI / Environmental Monitoring
Pyrrole Solution Flash Point and Melting Point
Bovine Rotavirus Efficacy Testing
Pharmaceutical Drug Gel Bloom Value
FDA GLP BA/BE Animal Health Generic Drug Study
Bioavailability and Absorption Studies
Permethrin Transfer Rate
Blood Tetrahydrocurcumin Analysis
FDA GLP Chronic safety studies
In Vivo Oxygen or Air Permeability
Preclinical Therapeutical Radiopharmaceutical Toxicology Studies
Plasma Protein Binding Studies
FDA cGMP BSL-2 Tap Density
Biopharmaceutical Cicular Dichroism Experiments
In-Vivo General Safety and Pyrogen Testing
Containment Performance Testing
Condom Biological, Toxicity, Microbiology and Packaging Studies
Pharmaceutical Third-Party QC Evaluation
Preclinical Hair Growth Study
Pharmaceutical Gel Viscosity
FDA GMP Biopharma Container Closure Testing
USP Gentamicin Testing
In-Vitro Bioavailability Study
ISO Cytotoxic Infusion Pumps Polymer Degradation
Pharmaceutical OEB5 Molecule Characterization
Nootropic Compound Certificate of Analysis (COA)
Chemotherapy Drug Compatibility Testing
Pharma API Hygroscopicity testing
Opiod Receptor In Vitro Activity Study
Influenza Vaccine Challenge Study Testing
Doxepin Deformulation Testing
Diclofenac Sodium USP Research
Unknown Protein Peak Analysis
Small Molecule Competitive Enzyme Inhibitor
Medication Child Resistant Carton Testing
OECD Environmental Risk Assessment
USP Massage Oil Testing
Anabolic Steroids and Research Chemicals
Non-GLP Pharmacokinetic PK Studies
IV Bags USP Container Closure Integrity Testing
FDA Biopharmaceutical Release, Stability and Container Closure Integrity Testing
Pharmaceutical Excipient and Packaging Testing
Contract Research Organization In-Vivo Study
AOAC Sporocial and Disinfectant Efficacy Testing
Erucic acid- inherent plant toxins and Ergot sclerotia and ergo alkaloids
HIV-1 Genotyping for RT and Integrase
Pharm Eur Monograph Poloxamer 338
Buffer Chemical Analysis Services
Anti-Denque, Zika , Influenza and Zika
USP Pharmaceutical Testing
Gene Therapy Vector Copy Number
In Vivo Acute Toxicity and Product Safety Study
NF Monograph Dimethicone Validation Testing
ACTH and Corticosterone Testing
Pain Treatment Genetics test Study
Liquid Sunscreen Reverse Engineering / Deformulation
USP Pharmaceutical Osmolality Testing
Pharmaceutical Water Activity
Real Time polymerase chain reaction (qRT-PCR) assay
Weight Loss Accelerated Aging Study
USP Differential Scanning Calorimetry
USP Pharmaceutical Packaging testing
USP 41 - NF 36 Pharmaceutical Analysis
USP Pharmaceutical Stability Studies
ASTM Pharmaceutical Distribution/Transit Testing
Pharmaceutical Blend Concentrate Analysis
Government of Canada Pharmaceutical Equivalency Study
API Genotoxicity Testing
Nano-Sized Colloidal Intravenous Iron Preparation
Pharmaceutical USP Impurity Testing
Biologics Release Testing
Pericardium Patch Thrombogenicity Studies
Pharmaceutical Yellow Dye Raw Material Testing
URGENT Microbiology Confirmatory Study - 2500 samples
ISTA Pharmaceutical Packaging Testing
Generic Drug Pharmaceutical Physiochemical Testing
API Colloid Particle Characterization Analyses
Active Pharmaceutical Ingredient API Product Development
Shelf-Life Stability Studies
AOAC Inulin and FOS (Fructo-oligosaccharides) Testing
Nasal Solution Tonicity Testing
Anti-Viral Studies (CPV, IFV, VSV, BPSV)
Pharmaceutical Semi-Solid Pharmaceutical Reverse Engineering
Veterinary Medicine Sterile Injectable Pyrogen Testing
USP Blister Pack MVTR
Pharmaceutical Excipient Analysis
Pharmaceutical Gel Strength / Bloom Value
Pharmaceutical HPLC Impurity Determination
Pharmaceutical Oil Based Gel Suspension
Anti-HIV Activity throguh Protease Inhibition
Early Cancer Warning System Biomarker Testing
India Pharmaceutical Rheology Studies
HDPE FDA and MHRA Pharmaceutical Bottles and Cap Testing
Pharmaceutical Metals and Microbiology Testing
Modified EP Method Testing for Tobramycin
Pharmaceutical USP Elemental Impurities Method Development and Validation
USP Gelatin Powder Bloom Testing
Oral Solutions Organoleptic Properties
Propropiconasole Testing
Porcine Blood Nitrous Oxide Levels
USP Tribasic Calcium phosphate Testing
48 Hour Dermatological Patch Tests
FDA GMP Monoclonal Antibody Batch Release Testing
Opthalmic Pharmaceutical Deformulation
Pharmaceutical Chemotherapy Usability Lab Space
Zoledronic Acid Quantification
EPA and USP Polymer Characterization
European Pharmacopeia Rubber Stopper Penetrability Testing
FDA GMP Pharmaceutical Vapor Pressure
European Pharmacopoeia Sterile Pharmaceutical Release Testing
FDA GMP Veterinary Medicine Characterization
Essentival Oil Topical Pain Relief Oil
Suspension Microbial Analysis
FDA GMP Gene Therapy Lot Release
FDA GMP Personal Lubricant Laboratory Analyses
FDA GLP Ultrasound Gel Testing
FDA GMP Pharmaceutical Multi-Point Dissolution Studies
USP Calcitonin Salmon Bio-Identity Testing
European Pharmacopoeia Rubber Stopper Penetrability Testing
In vitro anti fungal efficacy test
FDA OTC Finished Drug Product Testing
Pharmaceutical Drug Comparison Study
Pharmaceutical USP Water Testing
Active Pharmaceutical Ingredient API Method Development and Validation
Pharmaceutical Containment Equipment Testing
Small Molecule, Polymer Based Drug Delivery System Method Development
DEA Impurity Isolation Characterization
Surfactant Critical Micelle Concentation
Europe Clinical Laboratory
Nasal Spray Preservative Efficacy Studies
Fondaparinux Sodium USP
IAS Special Packaging Testing
Potassium Iodide Shelf-Life Extension
Novel Compounds Inhibition Against NDM-1 Enzyme
Drug Product Degradation Product Structure Elucidation
Protein Comparison Study
Finished Release Bioassays
Small Molecule Pharmaceutical Analysis
USP Castor Oil Testing
Medical Device Wearables Wireless Coexistence Testing
Biomaterial MBEC Studies
USP DRUG SUBSTANCE NMR
Human Serum Quality Control QC Panel
Pharmaceutical In-Vitro Virue Neutralization Assays
Active Pharmaceutical Ingredient API Capillary Electrophoresis
Compounded Pharmaceutical Stability Studies
Peptides HPLC Analysis
GCP and MHRA/EMA Clinical Trial ELISA Assays
Breast Cancer Assays
FDA GMP OTC Hair Growth Toner Testing
Protein Circular Dichroism
HPLC, NMR, and MS Spectrums
Dimethyl Sulphate (DMS) in Drug Substance
Pharmaceutical Fluorescence Microscopy
N13-Ammonia Impurities
USP Pharmaceutical API Compendial Vertification
ABUSE-DETERRENT STUDIES
Stem Cell Genomic Stability Research
Pharmaceutical LCMS correlation and confirmation testing
Rhinovirus Research Study
Pharmaceutical Quality Control QC Testing
Waterproof Medical Grade Adhesive Reformulation
ICP-MS Elemental Analysis
USP Qualification of Chemical Entity for Clinical Trial
USP Heparin Monograph Testing
Anti-Lice Efficacy Testing
GLP/ICH Chronic Toxicity Study
Preclinical Drug Substance Characterization
Pharma Related Substances
Growth Promotion of Sweat Formulation
Topical Pain Ointment Deformulation
Recombinant HGH Quality
Preclinical Helicobacter Study
Transfection of SH-SY5Y Neural Cells with Candidate Plasmids.
Zonulin, Apo-A2, Bifidobacterium, Lactobacillus
Preclinical Oncology Contract Research Organization CRO
14C Radiolabeled USP Bacterial Endotoxin Testing
Hereditary Cancer and Pharmacogenetics
Pharmaceutical Deformulation / Reverse Engineering
Multiple OECD Studies
USP Soybean Oil Testing
FDA GMP Clinical Trial Paraben Testing
Tensile, Strain, Modulus and Relaxation
Quotation for EP 5.1.3 standards Antimicrobial Effectiveness Testing
Transdermal Patch Clinical Research
Identification: Chondroitin Sulfate Sodium
Lipids on Skin Analysis
Pharmaceutical Shipper Drop Testing
Qualitative Tuberculocidal Study
Container Closure Integrity Testing (CCIT)
Pharmaceutical Nanotechnology
Quantification of Drug in Lung tissue
SAE Polymeric Material Fluid Permeation
Cellular Adherence Study with HeLA, BAE, SH-SY5Y Cells
Plasma Bioanalysis
Viscosity Testing
GLP Preclinical Studies
Pharma API and Finished Drug Product Testing
FDA Clinical Trial Drug Application Testing
Anti-Fungal Toenail Ointment
Pharmaceutical Antiviral Efficacy
USP Protein Analysis
Biopharmaceutical Assays
UN Safety Testing
Medical Device Certificate of Friction
Residual Host Cell DNA by qpcr
Multiple Cannabis Packaging Products
Human Mucus Study
Residual Ampicillin
Pharmaceutical Excipient Analysis by Capillary Viscometer
Sunscreen Effects on Vitamin D Clinical Trial
OECD Genotoxicity Study
Pharmaceutical Packaging Testing
Medication Testing
GLP In-Vitro Release Testing (IVRT) Comparative Studies
Peripheral Blood Mononuclear Cell (PBMC)
Pharmaceutical Deformulation Study
Pharmaceutical / Medical Device DSC Analysis
MHRA and FDA approved Laboratory
Toxicity Studies
Pharmaceutical Drug Packaging
Pharmaceutical Cytotoxic Drug
Pharmaceutical Excipient USP Monograph
Cancer Research Study
Benzocaine Impurities
Western Blot of Human Skin Protein
In vitro exon skipping study
Starch Brabender Testing
Drug Anti-Pyretic Study
Pharmaceutical Cyanide Content
CLIA Biomarker LC-MS/MS
Albumin Zone Electrophoresis
Pharmaceutical Disintegration and Dissolution
Pharmaceutical Confirmation Testing
USP Surface Area Analysis
Peptide ID Confirmation & Purity Assay
Insulin Analysis
Pharmaceutical Nasal Spray Droplet Size
Pharmaceutical Container Closure Integrity
Drug Inhalation Release
Pharmaceutical Osmolality Testing
FDA Sunscreen Testing
CRO with human in vitro neuromuscular junction assay (NMJ) system
Disinfectant Comparative USP Efficacy Sutdy
Preclinical IND Enabling Safety Studies
Small Batch Formulation, Development and Testing
Multi-Lab Precision Study of an In-Vitro Diagnostic
Electron Capture Detection of Halogenated Compounds
Clinical Trial
Pharmaceutical Aerosol Testing
OTC Drug Testing
NIH Vaccine Potency Testing
Custom Peptide USP Testing and Validation
FDA cGMP Particle Size
Pharma Hydroxyl Number Testing
Trimethylamine-N-oxide TMAO Analysis
USP Compendial Testing
CaCo3 masterbatch testing
USP Validation and USP <787> Subvisible Particulate Matter in Therapeutic Protein Injections
Tumorigenesis Study
Drug API and Finished Formulation Testing
Clinical Trial Amino Acid Analysis
Drug Product Compatibility Testing
USP Assay of Sennosides
Bioassays for Sucralfate
X-Ray Diffraction Analysis
USP Residual Solvent Testing
Antibody Testing
SMEPAC / Surrogate Process Performance Study
USP Monograph Analysis of Oxytocin
CCR Packaging Testing of Healthcare Caps and Jug Containers
Anti-viral drug Testing / Virus-neutralizing monoclonal antibody
GMP Compliant Surface Area Testing of Drug Substances
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