Continuous Improvement in Cleaning Validation Drive continuous improvement in cleaning validation processes with our tailored solutions. Our offerings include: * Analysis of cleaning validation data to identify trends and areas for improvement * Implementation of corrective and preventive actions (CAPA) to address deficiencies and enhance cleaning processes * Training and education programs to enhance employee competency in cleaning validation techniques and regulatory requirements ?? Website: www.compleatts.com ?? Email: [email protected] ?? Phone: +1 (704) 453-8093 #CleaningValidation #ContinuousImprovement #CAPA #ProcessOptimization #RegulatoryCompliance #QualityAssurance #EmployeeTraining #ManufacturingExcellence #ValidationSolutions #OperationalExcellence
Compleat Technical Solutions Inc
人才中介
Deploying right talent at the right time and tailor-made solutions
关于我们
At Compleat Technical Solutions INC, we specialize in providing comprehensive workforce solutions tailored to the needs of the biotechnology, pharmaceutical, medical device, and IT industries. With expertise in recruitment for Quality, Validation, Regulatory Affairs, and IT, we are dedicated to supporting life science companies throughout the entire CQV (Commissioning, Qualification, and Validation) lifecycle. Our team of professionals excels in delivering Validation support across various areas including CQV/Equipment Validation, Process Validation, Cleaning Validation, Computer Systems Validation, Analytical Lab Equipment Validation, Calibration, Preventive Maintenance, and Regulatory Affairs. We understand the critical importance of compliance and efficiency in highly regulated industries, and our services are designed to ensure adherence to industry standards and regulations. Here's what we specialize in: ? Facilities Equipment ? Utilities Equipment ? Processes ? Cleaning Validation ? Test Method Validation ? Greenfield CQV Projects ? New Production Suite Commissioning ? Decommissioning ? End-to-End Solutions ? Project Planning ? Validation Master Plans (VMP) ? User Requirements Specifications (URS) ? Risk Assessments ? Protocols (FAT, SAT, etc.) ? Summary Reports ? Traceability Matrix ? Calibration Matrix ? SOPs ? Integrated Commissioning and Qualification (ICQ) ? Validation Protocol Format ? Design Qualification (DQ) ? Installation Qualification (IQ) ? Operational Qualification (OQ) ? Performance Qualification (PQ) ? Good Automated Manufacturing Practice (GAMP) ? Current Good Manufacturing Practice (cGMP) Review ? Continued Process Verification (CPV) ? Pre-Operational Verifications ? Commissioning and Startup ? Technical Audits and Due Diligence Connect with us today to learn more about how we can elevate your operations and drive excellence in quality, validation, and regulatory compliance!
- 网站
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https://www.compleatts.com/
Compleat Technical Solutions Inc的外部链接
- 所属行业
- 人才中介
- 规模
- 11-50 人
- 总部
- Charlotte
- 类型
- 私人持股
地点
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主要
3440 Toringdon Way
US,Charlotte,28277
Compleat Technical Solutions Inc员工
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Sri Charan T
Validation Engineer (Process and Equipment ) at Compleat Technical Solutions Inc
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Challa Kiran
Senior Pharma and Medical Devices Recruiter
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Namita Vishwanathan Menon
Solar & BESS Development Projects | Project Manager @non-profit Energy-Analysis | Finance | Sustainability | AI in Energy
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Akhil Tadanki
Senior Life Sciences Recruiter | Hiring for USA| Mechanical Engineer | Validation Engineer | Manufacturing Engineer | Process Engineer | Bio Medical…
动态
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"Ensure Thorough Cleaning Coverage! Our Riboflavin Spray Ball Coverage Tests: - Apply riboflavin solution to equipment surfaces - Visualize coverage with UV light - Identify areas for optimization Optimize your cleaning processes! #CleaningValidation #RiboflavinTesting #QualityAssurance"
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"May the Divine Light Shine Upon You! Happy Janmashtami from our family to yours! May this auspicious occasion bring joy, prosperity, and spiritual growth. #Janmashtami2024 #KrishnaBirthday #BlessingsAbound"
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Sterilization Cycle Development Optimize your sterilization processes with our expert cycle development services. Our team offers: * Development of sterilization cycle parameters based on equipment design and product requirements * Validation of sterilization cycles to ensure microbial inactivation and product safety * Performance of heat distribution studies and biological indicator testing to verify sterilization effectiveness ?? Website: www.compleatts.com ?? Email: [email protected] ?? Phone: +1 (704) 453-8093 #SterilizationProcess #CycleDevelopment #SterilizationValidation #ProductSafety #MicrobialInactivation #BiologicalIndicatorTesting #HeatDistribution #QualityControl #RegulatoryCompliance #ManufacturingExcellence #CleanManufacturing
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?? Compleat Technical Solutions Wishes You a Joyous Raksha Bandhan! ?? On this special occasion of Raksha Bandhan, we honor the bonds of trust, protection, and unity that we share with our clients and colleagues. Just as a Rakhi symbolizes a promise of care and support, Compleat Technical Solutions is committed to safeguarding your business interests with our comprehensive technical services. Let's continue to support each other, much like the bond between siblings, fostering a collaborative environment where innovation and growth flourish. Wishing everyone a happy and prosperous Raksha Bandhan! ??? #RakshaBandhan #CompleatTechnicalSolutions #ClientCare #BusinessSupport #TechPartners
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"Happy Independence Day! Today, we celebrate the freedom and bravery that makes our nation proud. May the spirit of independence inspire us to stand strong, unite, and strive for a brighter future. Wishing you and your loved ones a joyous Independence Day! #IndependenceDay #Freedom #Pride #NationPride #CelebrateIndia #UnityInDiversity"
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MACO Calculation Precision Determine maximum allowable residue limits (MACO) with our precise calculation methods. Our consultants excel in: * Calculation of MACO values based on product safety and regulatory requirements * Consideration of factors such as therapeutic dose, toxicity, and analytical sensitivity in MACO calculations * Documentation of MACO calculations in cleaning validation reports for regulatory submission and compliance purposes ?? Website: www.compleatts.com ?? Email: [email protected] ?? Phone: +1 (704) 453-8093 #MACOCalculations #ResidueLimits #CleaningValidation #RegulatoryCompliance #PharmaValidation #ProductSafety #ToxicityAssessment #AnalyticalSensitivity #RegulatorySubmission #PharmaceuticalManufacturing #ValidationExperts
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"Boost cleaning validation! - Validate manual & automated cleaning - Customize protocols for your equipment - Verify residue removal Ensure effective cleaning! ?? Email: [email protected] ?? Phone: +1 (704) 453-8093 ?? Website: www.compleatts.com #CleaningValidation #ResidueRemoval #ValidationProtocols #ManualCleaning #AutomatedCleaning #EquipmentValidation #Compliance #QualityAssurance #PharmaManufacturing #ProcessOptimization #EffectiveCleaning #ValidationSupport
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Rigorous CIP/COP Validation Optimize your Clean-in-Place (CIP) and Clean-out-of-Place (COP) processes with our rigorous validation services. Our consultants offer expertise in: ● Validation of CIP/COP procedures for various equipment configurations and cleaning agents ● Development of robust cleaning validation protocols to ensure thorough cleaning and compliance with regulatory requirements ● Conducting risk assessments to identify potential cleaning challenges and develop mitigation strategies ● Verification of cleaning effectiveness through visual inspection, rinse/sampling analysis, and microbial testing ?? Website: www.compleatts.com ?? Email: [email protected] ?? Phone: +1 (704) 453-8093 #CIPValidation #COPValidation #CleaningValidation #RegulatoryCompliance #ManufacturingOptimization #CleaningProtocols #RiskAssessment? #MicrobialTesting #QualityAssurance #PharmaManufacturing #ProcessOptimization #ValidationServices #EquipmentCleaning #ComplianceExperts #CleaningEffectiveness
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Comprehensive Cleaning Validation Support Ensure the cleanliness and compliance of your manufacturing processes with our comprehensive cleaning validation support. Our team specializes in validating various cleaning methods to meet regulatory standards and ensure product quality. Here's how we can assist: ● Validation of Clean-in-Place (CIP), Clean-out-of-Place (COP), and manual cleaning procedures to ensure thorough removal of residues from equipment surfaces ● Expert validation of automated cleaning systems for efficiency and consistency in cleaning processes ● Conducting rinse and swab analysis to verify the effectiveness of cleaning procedures and ensure residue levels are within acceptable limits ● Thorough testing of Total Organic Carbon (TOC) levels to assess the cleanliness of equipment and verify compliance with regulatory requirements ● MACO (Maximum Allowable Carryover) calculations to determine the maximum allowable residue limits for products manufactured on shared equipment ● Development of CIP and sterilization cycle parameters to ensure effective cleaning and sterilization of equipment ● Riboflavin spray ball coverage tests to evaluate the efficiency of cleaning coverage and identify any areas of insufficient cleaning ● Inclusion of other critical events in cleaning validation, such as equipment disassembly/reassembly procedures, cleaning agent compatibility testing, and validation of cleaning equipment performance ?? Website: www.compleatts.com ?? Email: [email protected] ?? Phone: +1 (704) 453-8093 #CleaningValidation #CIPValidation #COPValidation #ManufacturingCompliance #RegulatoryCompliance #ProductQuality #EquipmentCleaning #RinseAnalysis #SwabAnalysis #TOCTesting #MACO #Sterilization #CleaningProcess #PharmaManufacturing #ValidationSupport #QualityControl