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ANDY

WDA(H) COMPLIANCE SOFTWARE

GDP compliance software
for WDA(H) holders.

ANDY helps pharmaceutical wholesalers turn regulatory guidance, controlled SOPs and operational evidence into cited, reviewable work—while the Responsible Person retains every accountable decision.

BUILT AROUND WHOLESALE DISTRIBUTION

Keep the evidence behind every GDP decision.

01

Ask the operational question

Start with the issue in front of you: a supply query, a return, an excursion, a qualification check or an inspection action. ANDY identifies the work and keeps the question attached to its context.

02

Ground it in the right sources

Work from approved regulatory material, your organisation’s controlled SOPs and documents attached to the assessment. Citations stay connected to the claims they support.

03

Make gaps and boundaries visible

Missing evidence, conflicting sources and RP decision points are surfaced inside the answer instead of being hidden behind confident wording.

04

Carry the work into review

Preserve the reasoning, collaborate on the recorded conversation and export working material for human review without presenting AI output as an approved quality record.

GDP questions WDA(H) operations Bona fide checks Deviation support Inspection preparation Cited evidence
CUSTOMER & SUPPLIER QUALIFICATION

Structure bona fide checks around current evidence.

Bring authorisation evidence, product scope, site details and approval rationale together so the RP can review how a trading partner was qualified and when it needs checking again.

DEVIATIONS & EXCURSIONS

Assess what happened before deciding disposition.

Separate observed facts from assumptions, identify the evidence still required and keep final stock-status decisions with the authorised person.

INSPECTION PREPARATION

Connect readiness questions to the evidence behind them.

Use controlled procedures and workspace activity to organise open CAPAs, training records, self-inspection work and the context behind previous actions.

CONTROLLED KNOWLEDGE

Keep company procedure distinct from regulation.

Manage approved SOP versions with role-aware visibility and show whether an answer comes from published guidance, an internal procedure or an attached working document.

Software beside the RP—not software acting as the RP

ANDY does not hold the wholesale dealer’s authorisation, approve suppliers or customers, release returned stock, close deviations or certify compliance. It organises evidence and working analysis so authorised people can make and record better-informed decisions.

QUESTIONS, ANSWERED

Clear about the boundary.

No. ANDY provides evidence-led decision support and working material. The Responsible Person and other authorised people retain their legal, professional and organisational responsibilities.

Yes. Plans that include the SOP library let teams manage controlled document versions with status and visibility controls, so answers can distinguish internal procedure from published regulatory evidence.

ANDY can structure the qualification assessment, bring evidence and requirements together, and preserve the rationale. Approval and any decision to trade remain with your authorised process and people.

ANDY is an evidence and compliance workspace rather than a claim to replace every eQMS function. It can sit alongside established quality systems by supporting research, analysis, controlled knowledge and reviewable drafting.

READY WHEN YOU ARE

Put ANDY
beside your RP.

Start with a focused workspace for day-to-day compliance work, then bring your team and controlled knowledge with you.

View plans