eQMS
Electronic Quality Management
Track deviations, corrective actions and controlled changes. Useful when quality investigations and approvals span several teams.
Discuss your needsBusiness Solutions
Pharma & Life Sciences Solutions
Connect quality, laboratory and manufacturing workflows with AmpleLogic solutions, delivered through SITEC in Jordan and the Levant.
Explore the scope
LOCAL EXPERTISE. CONNECTED SOLUTIONS.SITEC — Authorized AmpleLogic Reseller in Jordan & the Levant
FROM WORKFLOW TO VISIBILITY
Connected quality, laboratory and manufacturing.
Scattered records and disconnected approvals make everyday work harder to follow. Start with your operational priorities and explore the modules that help your team organize them.
Controlled documents, relevant training and clear approvals support work across teams.
01
Quality & Documentation
DMS
Document Management
Manage review, approval and document versions. Useful when staff need reliable access to current SOPs and work instructions.
Discuss your needsLMS
Learning Management
Organize training and qualification records. Useful when responsibilities or procedures change and training completion must be tracked.
Discuss your needs02
Laboratory Operations
LIMS
Laboratory Information Management
Follow samples, tests and reviewed results in one workflow. Useful for QC teams managing sample volumes and laboratory traceability.
Discuss your needsELN
Electronic Laboratory Notebook
Structure experimental records and scientific observations. Useful when laboratory knowledge needs to be documented and shared consistently.
Discuss your needsStability
Stability Management
Organize stability studies and their results. Useful when teams need visibility across product stability programmes.
Discuss your needsQC Planning
QC Planning & Scheduling
Coordinate laboratory work schedules. Useful when competing testing priorities need a clearer execution plan.
Discuss your needs03
Manufacturing & Equipment
MES / eBMR
Manufacturing Execution & Batch Records
Digitize batch execution and records. Useful when production teams are moving away from paper batch documentation.
Discuss your needseLogbook
Electronic Logbook
Replace paper operational logbooks. Useful when routine entries need more consistent recording and retrieval.
Discuss your needsCAPS
Calibration & Preventive Maintenance
Coordinate calibration and preventive maintenance schedules. Useful when equipment activities need systematic follow-up.
Discuss your needsCVS
Cleaning Validation
Organize cleaning validation assessments and records. Useful when shared equipment requires documented cleaning strategies and review.
Discuss your needs04
Quality Intelligence & Regulatory Operations
APQR
Annual Product Quality Review
Bring product quality data together for periodic review. Useful when annual reports require lengthy collection from multiple teams.
Discuss your needsCPV
Continued Process Verification
Review process trends and variation. Useful when manufacturing teams need ongoing evidence of process performance.
Discuss your needsRIMS
Regulatory Information Management
Organize product registrations, approvals and renewals. Useful when regulatory teams coordinate submissions across markets.
Discuss your needsUAM
User Access Management
Centralize user access management. Useful when access responsibilities need clearer control across regulated systems.
Discuss your needsStart with the module that meets your priority.
We help select relevant modules and coordinate a suitable demonstration, then define integration, training and validation needs before expansion.
Explore also: Business Process Automation · Official AmpleLogic portfolio
ABOUT THIS SERVICEBack to all services in this area
Pharma & Life Sciences Solutions
Paper records, scattered spreadsheets and disconnected approvals make it harder to trace decisions and prepare evidence for review. AmpleLogic offers specialized modules for pharmaceutical and life sciences operations. SITEC works with your team to identify priorities and select the relevant modules, with implementation scope, integrations and responsibilities agreed for your environment.
Start with the workflow that needs attention
Begin with document control, quality events, laboratory work or production records, then plan expansion around the value and dependencies of each module. Existing ERP, equipment interfaces and data sources should be assessed before committing to integrations.
Technology supported by a clear validation plan
Electronic records, access controls and approval workflows can support regulated operations. Compliance also depends on configuration, validated use, procedures and training. Your quality team and AmpleLogic should agree the validation requirements and evidence for the selected scope; software alone does not confer regulatory approval.
SERVICE SCOPE
01Workflow and module selection
02Implementation scope and integration planning
03Coordination with AmpleLogic and the client’s quality team
04Training and validation requirements planning
05Phased adoption and expansion
Technologies we deliver with
1 leading technology partners across this solution.
SITEC Jordan
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