Research – Page 12

Peptide Clinical Trial Endpoints: Choosing Measures That Answer the Question

Endpoint quality depends on interpretability, measurement reliability, and protocol execution together.

An evidence-first guide to endpoint definition, estimands, measurement quality, and operational readiness in peptide trials.

Peptide Cold-Chain Handling: Research Controls for Storage and Transport

Cold-chain integrity is a chain of controlled decisions from receipt through use.

How peptide teams can build temperature, excursion, inventory, and chain-of-custody controls around stability-sensitive materials.

Peptide Comparability Analytics: What to Compare After a Process Change

Comparability asks whether a change introduced a meaningful difference across relevant quality attributes.

A practical research framework for comparing peptide material across process, site, scale, formulation, or analytical changes.

Peptide Impurity Profiling: From Sequence Risk to Quality Decisions

Peptide impurity control starts with understanding how chemistry and process conditions create the profile.

An evidence-first guide to peptide-related impurities, analytical coverage, toxicology questions, and documentation.

Lyophilization Development for Peptides: Formulation and Cycle Evidence

Lyophilization development balances product temperature, cycle time, reconstitution, and long-term stability.

Research priorities for peptide freeze-drying, including formulation screening, cycle design, reconstitution, and stability evidence.

Peptide Pharmacokinetic Sampling: Designing Interpretable Exposure Data

Pharmacokinetic conclusions are limited by sampling design, assay meaning, and specimen integrity together.

An evidence-first look at sampling windows, bioanalysis, specimen handling, and interpretation in peptide pharmacokinetic studies.

Peptide Research Data Integrity: Controls for Modern Laboratory Workflows

A research result is only as durable as the record that allows another reviewer to reconstruct it.

A practical guide to attributable, legible, contemporaneous, original, and accurate peptide research records across digital systems and contract labs.

Peptide Research Grant Administration Workload 2026

A practical workload model for grant calendars, documents, reporting, and research-team handoffs.

Peptide Literature Review Workflows: From Search Strategy to Reproducible Brief

Decision-ready literature reviews make search scope, screening, and uncertainty visible.

A research-operations workflow for systematic searching, evidence grading, citation management, and decision-ready peptide literature briefs.

Peptide Research Literature Screening Workload 2026

A practical research brief on screening, triage, and documentation workload for peptide teams.

Peptide Research Study Startup Coordination 2026

An operational research brief on study startup calendars, document readiness, and research-team handoffs.

Stability-Indicating Methods for Peptide Programs: Research 2026

Stability conclusions depend on demonstrated specificity, not a single passing assay result.

How peptide teams can connect degradation pathways, analytical methods, forced degradation, and shelf-life evidence.