{"id":5350,"date":"2025-10-31T01:05:25","date_gmt":"2025-10-30T22:05:25","guid":{"rendered":"https:\/\/logo-tasarimci.com.tr\/?page_id=5350"},"modified":"2026-04-01T17:16:08","modified_gmt":"2026-04-01T14:16:08","slug":"in-house-trainings","status":"publish","type":"page","link":"https:\/\/qualityacademia.com\/tr\/in-house-trainings\/","title":{"rendered":"In House Trainings"},"content":{"rendered":"
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\r\n \r\n <\/i>\r\n \r\n In House Trainings\r\n \r\n <\/span>\r\n <\/h3>\r\n <\/div>\r\n<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Exemplar Global \u2013 Accredited & Industry-Focused Trainings<\/h4><\/td><\/tr>

Training Title<\/td>Duration<\/td>Availability<\/td>Request a Quote<\/td>Enroll<\/td><\/tr>
Risk-Based Best Practices in Change Control<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Deviations, Corrective & Preventive Actions (CAPA)<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
GMP Fundamentals<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Advanced GMP Practices<\/td>3 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Train-the-Trainer: GMP Instructor Development<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Quality Risk Management with Practical Case Studies<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Behavioral GMP & Quality Culture in Pharmaceutical Manufacturing<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Root Cause Investigation & Human Error Prevention Techniques<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Annual Product Review (APR) and Trend Analysis<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Process Validation & Lifecycle Approach (FDA, EMA, PIC\/S, T\u0130TCK)<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Sterile Manufacturing<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Supplier Qualification<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Technology, Test Method & Product Transfer<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Computerized System Validation (CSV)<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Cleaning Validation & Lifecycle (Including PDE\/ADE Concepts)<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based HVAC, Water, Steam & Gas Systems Validation<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/td>\u2705<\/a><\/td><\/tr>
Environmental Monitoring & Contamination Control Strategy for Sterile Manufacturing<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Analytical Method Validation & Equipment Qualification<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Best Practices in Microbiology Laboratory<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Temperature Mapping for Warehouses & Cold Rooms<\/td>2 Days<\/td>All Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
GDP-Compliant Route Qualification for Pharmaceutical Transport<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
GDP-Compliant Vehicle & Warehouse Qualification<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Sampling Plans<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Advanced Stability Studies<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Facility Layout Design & GMP-Compliant Engineering Applications<\/td>3 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
21 CFR Part 11 & EU GMP Annex 11: Electronic Records and Signatures<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Data Management & Data Integrity (with Case Studies)<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Elemental Impurities & Pharmaceutical Impurity Profiling<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Facility Management During Shutdown Periods<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Statistical Process Control (SPC) in Pharma & Biotech<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Best Practices in Quality Control Laboratories<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Best Documentation Practices for Pharmaceutical QMS<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Effective Training Design for Pharmaceutical & Biotechnology Industries<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Complaint Handling<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Out-of-Specification (OOS) & Out-of-Trend (OOT) Management<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Risk-Based Product Recall Management<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Operational Excellence (OPEX) Best Practices \u2013 Pfizer, Novartis, Novo Nordisk, Takeda, Abbott, Roche, Bayer<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Internal & Lead Auditor Programs (GMP, GDP, GQCLP, Data Integrity, Cleanroom)<\/td>Various<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>

Sterile & Biopharmaceutical Trainings<\/h4><\/td><\/tr>

Training Title (EN)<\/td>Duration<\/td>Availability<\/td>Request a Quote<\/td>Enroll<\/td><\/tr>
Sterile Product Development & Dosage Forms<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Sterile Product Technology Transfer<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Container-Closure Integrity Testing & Packaging<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Stability Studies for Sterile Products<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Operational Excellence (OPEX) in Sterile Products<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Air & Water Quality in Sterile Products<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Quality Risk Management in Sterile Products<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Visual Inspection in Sterile Products<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Filtration in Sterile Products<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Sterilization Methods & Validation<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Environmental Monitoring & Contamination Control for Sterile Products<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Microbial Flora Determination in Sterile Products<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Pyrogen & Endotoxin Testing in Sterile Products<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Bioburden, Sterility & Sterility Assurance<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Terminal Sterilization Methods<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Isolator & RABS Technologies & Containment<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Aseptic Process Simulation<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
PUPSIT (Product, Unit, Process Simulation & Integrity Testing)<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Lyophilization<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Single-Use Systems in Biopharmaceutical Manufacturing<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Biopharmaceutical Facility QMS Implementation & Management<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Downstream & Upstream Processing<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Master Cell Bank & Working Cell Bank<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Cell Culture & Protein Expression<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Filtration & Purification in Biopharmaceuticals<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Data Integrity & Management in Biopharmaceuticals<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Chromatographic Data System Validation in Biopharmaceuticals<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Analytical Method Validation in Biopharmaceuticals<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Process Validation in Biopharmaceuticals (FDA & EMA Approaches)<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Cleaning Validation in Biopharmaceuticals<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Bioreactor Design & Fermentation<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Biopharmaceutical Manufacturing Methods & Risk Assessment<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Biopharmaceutical Product Licensing & Regulatory Pathways<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Biosimilars & Biobetters<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
CIP & SIP (Clean-In-Place \/ Sterilization-In-Place) in Biopharmaceuticals<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Biopharmaceutical Facility Design & Validation<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Immunogenicity<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
International Guidelines, Regulations & Expectations for Sterile Products<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
PIC\/S GMP Guide & Annexes for Sterile Products<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/td><\/tr>
Lean Biopharmaceutical Manufacturing<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Worker Health, Safety & Environmental Management in Biopharmaceutical Manufacturing<\/td>1 Day<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Preparing Sterile Product Facilities for International Audits<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Supply Chain Management in Sterile Products<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr>
Transport, Storage & Distribution Requirements for Biopharmaceutical Products<\/td>2 Days<\/td>Pharma\/ Biotech<\/td>\u2705<\/a><\/td>\u2705<\/a><\/td><\/tr><\/tbody><\/table>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"

In House Trainings Exemplar Global \u2013 Accredited & Industry-Focused Trainings Training Title Duration Availability Request a Quote Enroll Risk-Based Best Practices in Change Control 2 Days Pharma\/ Biotech \u2705 \u2705 […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_EventAllDay":false,"_EventTimezone":"","_EventStartDate":"","_EventEndDate":"","_EventStartDateUTC":"","_EventEndDateUTC":"","_EventShowMap":false,"_EventShowMapLink":false,"_EventURL":"","_EventCost":"","_EventCostDescription":"","_EventCurrencySymbol":"","_EventCurrencyCode":"","_EventCurrencyPosition":"","_EventDateTimeSeparator":"","_EventTimeRangeSeparator":"","_EventOrganizerID":[],"_EventVenueID":[],"_OrganizerEmail":"","_OrganizerPhone":"","_OrganizerWebsite":"","_VenueAddress":"","_VenueCity":"","_VenueCountry":"","_VenueProvince":"","_VenueState":"","_VenueZip":"","_VenuePhone":"","_VenueURL":"","_VenueStateProvince":"","_VenueLat":"","_VenueLng":"","_VenueShowMap":false,"_VenueShowMapLink":false,"footnotes":""},"class_list":["post-5350","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/qualityacademia.com\/tr\/wp-json\/wp\/v2\/pages\/5350","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/qualityacademia.com\/tr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/qualityacademia.com\/tr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/qualityacademia.com\/tr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/qualityacademia.com\/tr\/wp-json\/wp\/v2\/comments?post=5350"}],"version-history":[{"count":56,"href":"https:\/\/qualityacademia.com\/tr\/wp-json\/wp\/v2\/pages\/5350\/revisions"}],"predecessor-version":[{"id":6446,"href":"https:\/\/qualityacademia.com\/tr\/wp-json\/wp\/v2\/pages\/5350\/revisions\/6446"}],"wp:attachment":[{"href":"https:\/\/qualityacademia.com\/tr\/wp-json\/wp\/v2\/media?parent=5350"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}